CN1232641C

CN1232641C - Modulator for function of receptor of TNF/NGF receptor family and other protein

Info

Publication number: CN1232641C
Application number: CNB998041513A
Authority: CN
Inventors: 大卫·沃勒克; 安德烈·科瓦连科; 马歇尔·S·霍维茨; 李永安
Original assignee: Yeda Research and Development Co Ltd; Albert Einstein College of Medicine
Current assignee: Yeda Research and Development Co Ltd; Albert Einstein College of Medicine
Priority date: 1998-03-19
Filing date: 1999-03-18
Publication date: 2005-12-21
Anticipated expiration: 2019-03-18
Also published as: EA004062B1; NO20004649L; IL126024A0; AU2954599A; SK13762000A3; NO327854B1; EP1062336A1; HK1034995A1; CA2323637A1; US6734174B1; KR100748293B1; NZ525566A; ATE318310T1; SK285804B6; BR9909659A; PL200763B1; JP4351389B2; CN1295614A; BG65684B1; DE69929958D1

Abstract

A new protein capable of modulating or mediating the intracellular activity of RIP in inflammation, cell survival and cell death pathways is provided. DNA encoding it, a method for its production and its uses are also provided.

Description

The conditioning agent of the function of TNF/NGF receptor family and other proteinic acceptor

Invention field

Generally speaking the present invention relates to belong to the control field of acceptor He its biological function of the super family of TNF/NGF.The acceptor of the super family of TNF/NGF comprises acceptor for example p55 and p75 Tumor Necrosis Factor Receptors (TNF-Rs hereinafter is called p55-R and p75-R) and FAS ligand receptor (be also referred to as FAS/APO1 or FAS-R and hereinafter will be called FAS-R) and other.Especially, the present invention relates to be attached to other proteinic new protein, described other protein is member and the interior protein of regulating of other born of the same parents that itself directly or indirectly is attached to the TNF/NGF receptor family.

More particularly, protein and its homotype, fragment, derivative and the protein that is attached to RAP-2 that relate to a kind of RAP-2 of being referred to herein as (for RIP-related protein-2).

RAP-2 is attached to RIP (" receptor interacting protein matter ") thereby and can regulates or mediate the function of RIP and also can directly or indirectly regulate or mediate other the proteinic function that directly or indirectly is attached to RIP.The RAP-2 conjugated protein is the conditioning agent/mediation agent of RAP-2 function.

The background technology of association area

Tumour necrosis factor (TNF-α) and lymphotoxin (TNF-β) (hereinafter are called TNF, relate to TNF-α and TNF-β) be that main being bitten by monocyte gulps down plastidogenetic multi-functional struvite cytokine, its definition cell has many effect Wallach, D. (1986) are referring to Interferon, rabbit 7 (Ion Gresser, ed.), pp.83-122, academic press, London; With Beutler and Cerami (1987).TNF-α and TNF-β start its effect by being attached to specific cell surface receptor.Some effects help organism: for example they may damage the cell of tumour cell or virus infection and the antibacterial activity of increase granulocyte.By this way, TNF helps organism to the defence of antitumor and infectant with help recovery from injured.Therefore TNF can be used as antineoplastic agent, and it is attached to the acceptor of tumor cell surface in this application, takes place thereby start the situation that causes death of neoplastic cells.TNF also can be used as anti-infection agent.

But TNF-α and TNF-β also have deleterious effects.Excessive being created in that evidence suggests TNF-a plays main pathological effect in several diseases.For example, mainly having effect INF-α known to vascular system is chief reason people such as (, 1986) Tracey of sapremic shock symptom.In some diseases, TNF by suppress the active of adipocyte and by cause anorexia can cause the too much loss of body weight (emaciation) and therefore TNF-α be called as cachetin.Also it is described as in rheumatismal disease organizing prejudicial mediation agent (Beutler and Cerami, 1987) and as the mediation agent of observed infringement in transplanting-right-host response people such as (, 1987) Piquet.Known in addition TNF participates in the process of inflammation and many other diseases.

The biological action that begins and/or mediate above-mentioned TNF in conjunction with two different p55 of expressed receptor independently and the p75 TNF-Rs of TNF-α and TNF-β specifically.This can have different intracellular region territories on the receptor structure, show their form different signals (referring to people such as Hohmann, 1989; People such as Engelmann, 1990; People such as Brockhaus, 1990; People such as Leotscher, 1990; People such as Schall, 1990; People such as Nophar, 1990; People such as Smith, 1990; With people such as Heller, 1990).But the cell principle that set forth to participate in becoming in p55 and the p75 TNF-Rs born of the same parents signal so far is range protein and other possible factor for example.Form signal in Here it is the born of the same parents, appear at part usually and be after TNF (α or β) and the receptors bind, its effect is finally to cause in the beginning of replying cascade reaction of observed cell to TNF.

For the cytosis of killing of specific TNF above so far in the most cells of research, this effect is main by p55 TNF-R triggering.The antibody in the intracellular region territory (ligand binding region) of anti-p55 TNF-R itself can trigger cytosis (referring to EP412486) extremely, and this it is believed that it is the first step that the signal forming process in the born of the same parents produces with relevant by the effect of the cross-coupled acceptor of antibody.Thereby, the research of sudden change verified (people such as Brakebusch, 1992; People such as Tartaglia, 1993) biological function of p55 TNF-R depends on the globality in its intracellular region territory.Therefore, hinted cause TNF kill cytosis show that signal forms begin that to occur be because the result of the association in one or more p55TNF-R intracellular regions territory.And TNF (α and β) appears at the form of homotrimer, has so hinted by means of p55 TNF-R and has induced the formation that shows signal according to the ability of its combination and cross connection this receptor molecule, promptly causes the acceptor cohesion.

Another member of the acceptor of the super family of TNF/NGF is FAS acceptor (FAS-R), also it is referred to as FAS antigen, has homology at the cell surface proteins of various tissue expressions with the member of the cell surface receptor that comprises TNF-R and NGF-R.FAS-R mediated cell death in apoptosis people such as (, 1991) Itoh, and show the negative selective agent that is used as autoreaction T cell, promptly in the ripening process of T cell, the programmed cell death of the self antigen of FAS-R mediation T cell recognition.The sudden change that has also drawn FAS-R gene (lpr) causes the lymphopoietic disorder of mouse, and this is similar to the lupus erythematosus of people's autoimmune disorders system (SLE) (people such as Watanabe-Fukunaga, 1992).The part of FAS-R is the relevant molecule (cytotoxic T lymphocyte CTLs) of the cell surface that carries of lethality T cell seemingly, and therefore as CTLs and when carrying the cells contacting of FAS-R, they can induce the apoptosis that carries the FAS-R cell.In addition, prepared monoclonal antibody, it is specific with FAS-R, and these monoclonal antibodies can be induced the apoptosis that carries the FAS-R cell, comprises the mouse cell FAS-R that the people by cDNA coding transforms people such as (, 1991) Itoh.

The applicant has prepared many approach (referring to embodiment, European patent EP186833, EP308378, EP398327 and EP412486 number application), these approach are by utilizing anti-TNF antibodies or being attached to cell surface bonded TNF-Rs by utilizing soluble TNF acceptor so that compete TNF, by the combine deleterious effect of regulating TNF of inhibition TNF with its acceptor.In addition, being attached to its acceptor based on TNF is that the effect of TNF inducing cell is needed, the approach that the applicant has prepared (referring to for example EP 568925)

Regulate the effect of TNF by the activity of regulating TNF-Ps.

Briefly, EP 568925 relates to the method for conditioning signal transduction and/or cracking TNF-Rs, thus peptide or other molecule can with acceptor itself or with the effector protein interaction of acceptor interaction, so regulate the normal function of TNF-Rs.For EP 568925, to have described outside the born of the same parents of p55 TNP-R, in the film and intracellular region territory has structure and the feature of the various mutant p55 TNF-P of sudden change.By this way, the zone in the aforementioned region of p55TNF-R is differentiated that the i.e. combination of part (TNF) and signal transduction subsequently and intracellular signal formation causes observing the effect of TNF pair cell to greatest extent in order to be that the function of acceptor is necessary.In addition, also described and separate and differentiate that protein, many approach of peptide or other factor, the described factor can participate in regulating or the activity of the TNF-R that coordinates.Separate and the such protein of clones coding, many approach of the dna sequence dna of peptide, described DNA is used to make up the expression vector that is used to produce these protein and peptide, with with TNF-R or with above-mentioned protein and peptide interaction be used to prepare antibody or its fragment, also disclose in EP 568925, wherein said protein or peptide are in conjunction with the various zones of TNF-R.But, the protein and the peptide of EP 568925 unqualified reality, the intracellular region territory that they are attached to TNF-Rs (for example, p55 TNF-R), it does not describe the two kinds of hybridization approach of zymic that separate and differentiate such protein or peptide, and described protein and peptide are attached to the intracellular region territory of TNF-Rs.Similarly, EP 568925 does not have openly can be attached to the protein or the peptide in the intracellular region territory of FAS-R.

Yet well-known, relevant acceptor FAS-R on tumour necrosis factor (TNF) acceptor and the structure owing to excite destructive activity in the stimulation of the part that white corpuscle produces and the cell, causes himself death, thus the mechanism of this excitation process still solve seldom.Mutation research shows that cells involved toxicity relates to the different zone of intracellular region (people such as Brakebusch, 1992 when FAS-R forms with p55 TNF acceptor (p55-R) signal; People such as Tartaglia, 1993; Itoh and Nagata, 1993).These zones (dead zone) have similar sequence.It is related that the dead zone of FAS-R and p55-R trends towards the oneself.Their oneself is related obviously promoted the necessary acceptor of startup that signal forms cohesion (referring to people such as Song, 1994; People such as Wallach, 1994; People such as Boldin, 1995), the high level expression of acceptor causes being independent of that the part signal forms excites people such as (, 1995) Boldin.

Similar with the effect of other receptor-inducible, take place by a series of protein-protein interaction by TNF acceptor and the necrocytosis of FAS-R inductive, cause from the transformation that excites of the final enzymatic effector function of being attached to of ligand-receptor, in this case, non-enzymatic protein-protein interaction has been illustrated in research work, the signal that this effect starts necrocytosis forms: tripolymer TNF or FAS-R ligand molecular combine with acceptor, tend to oneself related (people such as Brakebusch, 1992 by the regional motif of application; People such as Tartaglia, 1993; Itoh and Nagata, 1993), increased interaction of molecules in last its born of the same parents (people such as Boldin, 1995a), and induce two cytoplasmic protein (also can mutually combine) to acceptor intracellular region territory-MORT-1 (or FADD) to FAS-R (people such as Boldin, 1995b; People such as Chinnaiyan, 1995; People such as Kischkel, 1995) and TRADD be attached to p55-R (people such as Hsu, 1995; People such as Hsu, 1996).Three protein that are attached to FAS-R and p55-R intracellular region territory in dead zone participate in inducing of necrocytosis by acceptor by the allos in homology zone is related, and also activated cell death independently, these three protein are differentiated by two screening by hybridization programs of zymic.One of them is a protein, and (people such as Boldin 1995b) also is known as FADD (people such as Chinnalyan, 1995) to MORT-1, and it combines with FAS-R specifically.Second is that TRADD (also participating in people such as Hsu, 1995,1996) is attached to p55-R and the 3rd RIP (also participating in people such as Stanger, 1995), is attached to FAS-R and p55-R.Except being attached to FAS-R and p55-R, these protein also can interosculate, and this provides functional " talk mutually " (" cross-talk ") between FAS-R and the p55-R.These occur in conjunction with the motif by conservative sequence, and " dead regional molecule ", acceptor is the same with their related protein like this.In addition, though prove that MORT-1 spontaneously is attached to FAS-R in the mammalian cell in two hybridization tests of zymic, it is in conjunction with occurring over just after the receptor for stimulating, and hint MORT-1 participates in the startup that the FAS-R signal forms.MORT-1 does not contain the feature of any sequence motifs of enzymatic activity, therefore as if the ability of its activated cell death does not relate to the intrinsic activity of MORT-1 itself, but some are attached to other proteinic activation of MORT-1 and further work in the downstream of signal formation cascade.The cell expressing of the MORT-1 mutant of the verified N-terminal portions that loses this molecule stops Cytotoxic inducing (people such as Hsu, 1996 by FAS/APO1 (FAS-R) or p55-R; People such as Chinnalyan, 1996), show that this N-stub area shifts the signal formation that two acceptors kill cytosis by protein-protein interactions.

Therefore, " motif in dead zone " of acceptor p55-R and FAS-R and their three relevant protein MORT-1, RIP and TRADD be the position of protein-protein interaction seemingly.Three protein MORT-1, RIP and TRADD and p55-R and FAS-R intracellular region territory interact.By dead regional combine of its dead zone with these acceptors, related for its dead zone of RIP and TRADD also oneself, (though MORT-1 is in this difference on the one hand, the not self-association in its dead zone).MORT-1 and TRADD are attached to FAS-R and p55-R respectively and also interosculate in addition.And MORT-1 and TRADD are attached to RIP effectively.Therefore, three protein MORT-1 as if, the interaction between RIP and the TRADD is the part of total adjusting of forming of the intracellular signal by these three protein mediations.The interactional interference of these three intracellular proteins causes the adjusting that caused by this effect.For example, the TRADD inhibition that is attached to MORT-1 can be regulated the interaction of FAS-R-p55 TNF-R.In addition, except above-mentioned TRADD is attached to the inhibition of MORT-1, the interaction of FAS-R-p55 TNF-R can be further regulated in the inhibition of RIP.

The anti-specifically TRADD of monoclonal antibody in the dead zone of anti-p55-R and the binding site in RIP site also can be used for suppressing or stoping these combination of proteins, therefore cause FAS-R and p55-R between interactional adjusting.

Also find recently except above-mentioned described cell cytotoxicity and its by various receptor-mediated adjustings, its conjugated protein comprises FAS-R, p55-R, MORT-1, TRADD, RIP, MACH, Mch4, and G1, many such acceptors and its conjugated protein also participate in the active adjusting of the transcription factor NF-KB examined, and it is cells survival or becomes active crucial conditioning agent, is responsible for the control of many immunity and inflammatory response gene and expresses.For example, have been found that in fact TNF-α stimulates the activity of NF-κ B, therefore TNF-α can be in conjunction with two class signals in cell, dead and another kind of by by means of the anti-dead inductive cell of protection of NF-κ B inducible gene expression of one class activated cell (referring to Beg and Baltimore, 1996; People such as Wang, 1996; People such as Van Antwerp, 1996).Also reported similar dual effect for FAS-R (referring to as in people such as above-mentioned Van Antwerp, the reference of 1996 described effects).Therefore show on the various types of cytositimulations based on TNF-α and/or FAS-R part, between necrocytosis and cell survival, have fragile balance, the net result that stimulates depends in the cell which aspect is stimulated at utmost, a kind of situation causes death (usually because programmed cell death), and another kind of situation is to survive by the activity of NF-κ B.

In addition, the inventor also further illustrated recently the possible approach that TNF/NGF receptor family member activates NF-κ B (referring to people such as Malinin, 1997 and the various last reference that proposes of this paper; With No. 119133, the IsraeL patent application IL 117800 that is examining that owns together and IL).Briefly, it has proposed several members of TNF/NGF receptor family by common shifting coupling protein, and TRAF2 can activate NF-κ B.The protein kinase of newly illustrating (referring to people such as above-mentioned Malinin, 1997 and IL 117800 and IL 119133) that is referred to as NIK can be attached to TRAF2 and stimulate the NF-kB activity.In fact, verified (referring to people such as foregoing Malinin and IL application) expression in the NIK of kinase deficiency mutant cells causes producing in normal endogenous mode can not stimulate NF-κ B and also in the prevention of inducing the NF-kB activity by TNF by means of FAS-R, by TRADD, RIP and MORT-1 stop induce (it is the shifting coupling protein in conjunction with these acceptors p55-R and/or FAS-R acceptor) of NF-κ B.All these acceptor p55-R, p75-R, FAS-R and its shifting coupling protein MORT-1, TRADD and RIP directly or indirectly are attached to TRAF2, significantly regulate inducing of NF-κ B according to itself and NIK bonded ability.

After FAS-R and/or p55-R stimulation, as if in the above-mentioned conditioning agent protein of equilibrated that participates between necrocytosis and the existence, protein RIP has important effect.RIP (referring to people such as Stanger, 1995 and also referring to people such as Malinin 1997) is in the dead zone in its C-terminal zone, can with mode independently and also by with MORT-1, p55-R, the zygotic induction cytotoxicity in the dead zone of FAS-R and TRADD.RIP also has the protein kinase zone in its N-stub area and intermediate zone, and described intermediate zone it is believed that and can combine with TRAF2, induces thereby participate in NF-κ B.Therefore, the detail file that relate to the characteristic of RIP and sequence (DNA and amino acid) are listed in the above-mentioned open source literature (particularly people such as Stanger, 1995), are incorporated herein by reference.

TNF participates in one of the startup of host anti-virus defence and cytokine of adjusting, similarly, virus has been developed into and expressed the gene that its protein is regulated cytokine activity, it is believed that the existence that promotes the virus in the animal host with these virus proteins of regulating cytokine, proteinic one of thorough example that is studied like this is the E3-14.7K that comes from

C group

2 and 5 type adenovirus hominiss (Ad), and it has the strong antagonist of the cytolysis of TNF-mediation.

Form the purpose of the molecule composition of cascade for the signal that separates TNF, described composition hits E3-14.7K by means of the virus infection target, has separated human E3-14.7K conjugated protein recently (for the 14K interacting protein of FIP-2, Li by two kinds of screening by hybridization, Y. wait people, 1998).Find FIP-2 to himself immunotoxicity, and reverse to the Cytotoxic protective effect of E3-14.7K, by the overexpression inductive of TNFR-I or RIP.Discovery FIP-2 has some homologys with RAP-2.Total similar figures degree between RAP-2 and the FIP-2 is quite low, because (Fig. 3) of seeing from the shared arrangement of two aminoacid sequences.But become more remarkable in the specific regions homology facing to proteinic C-end, last actual homogeny is the 30C end amino acid.Noteworthy is that except C-end above-mentioned, the leucine zipper motif of the supposition of FIP-2 is RAP-2 camber conservative (different is Ile substituting to Ala).

The similar sequence that coding is related to the proteinic HYPL of being referred to as of Huntington ' s disease is registered at GenBank recently, theme as " Huntington interacting protein HYPL " (registration number AF049614), described disease seemingly with RAP-2 edge homology far away.But the document of describing proteinic function is also not open.

Recently by disclosed discriminatings of reporting mouse RAP-2 homology of people (1998) such as Yamaoka S..Differentiated the homology NEMO (for the basic conditioning agent of NF-κ B) of mouse by the retrieval of keyword, its regulates the activation that NF-κ B signal forms.The cytometaplasia body of the rat fibroblast that HTLV-I Tax-is transformed carries out qualitative, called after 5R, it to the NF-κ B activated of all tests stimulate (LPS, PMA, IL-I, TNF) slow in reacting, and carry out its genetic complementation effect.Because this program reclaims the proteinic cDNA of coding NEMO48kD.Based on these data, it is said that the SR cell lacks this protein, and it is the part of high molecular I κ B-kinase complex, and is that its external formation is needed, NEMO may with IKK β homodimerization and direct interaction.

No. 120485 patent specification of Israel discloses the protein of RIP-association, is referred to as RAP, and it is attached to RIP specifically and suppresses NF-κ B and induce.

No. 123758 patent specification of Israel relates to the relevant protein of another RIP that is referred to as RAP-2 with it, and it has identical or similar activity.

RAP-2 also is referred to as 303 or RAP-303 or RAT-303 according to the present invention.For the consistency reason referred to herein as RAP-2.

Summary of the invention

One of purpose of the present invention provides coding RAP-2 protein DNA sequence, and wherein RAP-2 protein can be attached to RIP, and described dna sequence dna comprises one of the following: (a) sequence as shown in Figure 1; (b) fragments sequence in the coding (a); Or (c) sequence of coding (a) or analogue (b), this (a) or analogue (b) are compared to have in aminoacid sequence with (a) or protein (b) and are no more than 10 variation, described each be changed to one and amino acid whosely substitute, remove and/or insert separately, described fragment or analogue can be attached to RIP.

One of purpose of the present invention provides the reproducible expression vector that comprises above-mentioned dna sequence dna.

One of purpose of the present invention provides new protein RAP-2, comprises all abnormal shapes, and its analogue fragment or derivatives thereof can be attached to rip protein (hereinafter referred to as ' RIP ').Because RIP can be directly or indirectly and inflammation, the cytotoxicity of cell, the coding mediation agent of necrocytosis interact for example p55-R and FAS-R, and shifting coupling or conditioning agent protein MORT-1 for example, TRADD,

MACH, Mch4, G1 and other interaction, for example, can influence by the FAS part being attached to its acceptor and TNF and be attached to the intracellular signal forming process that its acceptor (p55-R) starts by being attached to RIP new protein of the present invention, and new protein of the present invention is the conditioning agent of effect of the pair cell of p55-R and FAS-mediation.Thereby RIP also can interact with TRAF2 and can be directly or indirectly and the interaction of NIK, and RIP has the conditioning agent of participation NF-κ B inductive inflammation and cell survival approach like this.Equally, by means of FAS-R, p55-R and its regulate protein MORT-1 and TRADD can directly or indirectly induce NF-κ B and cell survival by being attached to RIP or being attached to RIP activated TRAF2, protein of the present invention also can be that to form approach by means of common or relevant intracellular signal be the mediation agent of cell survival process by operation, and wherein various above-mentioned protein operations are survived with inducing cell.Similarly, be attached to and RIP bonded TRAF2 for p75-R, new protein of the present invention also can be the active conditioning agent of the p75-R mediation of the relevant mediation of RIP-.

Another object of the present invention is to above-mentioned new RAP-2 protein, its abnormal shape, analogue, fragment provide derivative antagonist (antibody for example, peptide, organic compound, or even its abnormal shape), this antagonist can be used for suppressing the signal forming process, or more particularly, comprise the inflammatory cell cytotoxicity if desired, or the cell survival process.

Another object of the present invention is to use above-mentioned new RAP-2 protein, its abnormal shape, analogue, fragment and derivative, to separate and the qualitative other protein or the factor, it may participate in the adjusting of receptor active, for example can be attached to RAP-2 protein and influence its active other protein and/or separation and the new protein of discriminating, its analogue, fragment and derivative be attached on it at other acceptor in signal forming process middle and upper reaches or downstream and therefore they also participate in its function.

The present invention also provides the RAP-2 conjugated protein, and it can regulate/mediate the RAP-2 function.

The present invention also provides the method for producing above-mentioned RAP-2 protein, its fragment or functional analogue.

Another purpose of the present invention has provided and can import to cell and RAP-2 and possible special-shaped the combination or interactional inhibitor of RAP-2, this inhibitor can work the active effect that suppresses the RIP-association in cytotoxic process, therefore, if desired, to strengthen cell survival, or have the activity that in the cell survival process, suppresses the RIP-association, and therefore if desired, to add strong cytotoxicity.

And one of purpose of the present invention is to use new RAP-2 protein above-mentioned, its abnormal shape and analogue, fragment and derivative as antigen fragment to prepare its polyclonal antibody and/or monoclonal antibody.This antibody is in turn intended for from the new protein of different source purifying, for example cell extract or cell transformed system.

In addition, these antibody can be used for diagnostic purpose, for example are used for differentiating relating to by p55-R the disorder of FAS-R or other relevant receptor-mediated abnormal function.

A further object of the present invention has provided pharmaceutical composition, comprises above-mentioned new RAP-2 protein, its abnormal shape or analogue, fragment or derivative, and the pharmaceutical composition that comprises above-mentioned antibody or other antagonist.

According to the present invention, separated new protein RAP-2, RAP-2 can be attached to RIP or interact with RIP, and therefore it is active conditioning agent or mediation agent in the RIP born of the same parents.RIP participates in coded signal and forms adjusting or the mediation of regulating, the relevant approach of cytotoxicity or necrocytosis for example, wherein RIP itself has cytotoxicity and therefore many other relevant protein of necrocytosis, MORT-1 for example, TRADD, MACH, Mch4, G1, the direct or indirect combination of p55-R and FAS-R.For example RIP with direct or indirect mode by means of be present in RI fragment " dead zone " motif/module with all foregoing protein bound to or relevant with it; It is inflammation, cell survival or become another approach of active approach, wherein RIP directly or indirectly may have activation by means of the kinases motif or the zone that can be attached at RIP and RIP with NIK bonded TRAF2, they participate in the activation of NF-κ B directly successively, and its activation plays a key role in inflammatory and cell survival.In addition, p55-R can interact with TRADD and TRAF2 (by means of TRADD) and be important to the activation of NF-κ B also, thereby in the cell survival approach, and therefore by with FAS-R, the combination of TRADD and p55-R (by means of TRADD) and TRAF2 or interaction RIP also relate to the adjusting by these protein inflammation, the cell survival activation.Therefore, RIP is the conditioning agent or the mediation agent of these approach, and similarly, and by conditioning agent or the mediation agent that to be attached to RIP new RAP-2 of the present invention be approach in these born of the same parents.

Utilize two kinds of crossing systems to separate and cloned RAP-2, order-checking and qualitative, as mentioned below, RAP-2 seemingly high degree of specificity RIP conjugated protein and therefore specific RIP conditioning agent/mediation agent RAP-2 not with TRADD, MORT-1, p55-R, p75-R and MACH combination.As if further, RAP-2 does not have distinctive dead regions module or motif, the result of inducing cytotoxic is not inconsistent to itself for this result and RAP-2.

As used herein, the RIP activity means the adjusting/mediation that is included in inflammation and the necrocytosis survival approach.Above and hereinafter and described these activity in open source literature above-mentioned and the patent documentation, all documents are introduced into as a reference in full.Similarly, as used herein, the RAP-2 activity comprises owing to it combines the adjusting/mediation RIP activity that forms with the specificity of RIP.RIP by RAP-2 adjusting/mediation comprises inflammation, adjusting/the mediation of necrocytosis and cell survival approach, so RAP-2 can be regarded as above-mentioned protein and maybe may relate to inflammation, necrocytosis and survival and RIP in conjunction with or with the indirect regulation person and the mediation person of interactional some other material of direct or indirect mode.

The present invention also discloses the new RAP-2 conjugated protein that can utilize total length RAP-2 protein sequence to be differentiated by two screening by hybridization methods as bait.

Use total length RAP-2 protein as bait in two screening by hybridization methods, new RAP-2 interacting protein above and is hereinafter represented clone #10 (or clone's #10-encoded protein matter or RAT-conjugated protein #10 or RBP-10).By the sequence of the known common of the those skilled in that art cDNA that further extension is obtained to the sequence measurement of 5 ' end, to rebuild the proteinic part open reading frame that has lost initiator codon.

Two kinds of these protein of hybridization test shows of the whole projects of bonded of clone #10 not only combine with RAP-2, and show the great affinity of TRAF2.But clone #10 not with RIP, TRADD, MORT1, MACH, TNFR-1, the clone #10 that TIP60 and NIK and several Control protein bound (for example lamin and cyclinD) but get rid of in the born of the same parents found in mammalian cell combines NIK behavioural trait in the consideration yeast with NIK's.Proof clone #10 in 200 amino acid of the latter's C-end in conjunction with RAP-2, promptly with RAP, TIP60, NIK and IKK β are in conjunction with not necessary zone.But inaccurately two of this sequences make us carry out several GenBank of wheel retrievals, and purpose is to differentiate the homology of clone #10.Shown with the unique protein that has similarity degree in essence by clone's #10 encoded protein matter be the molecule that F40F12.5-comes from the supposition of C.Elegans, wherein do not assign physiological role.

What is interesting is, find some similaritys of several members of the high conservative family of F40F12.5 and ubiquitous proteolytic enzyme.These enzymes are the destructive effects of the ubiquitous mechanism of balance conversely, has known that this destruction bears the incident of most protein degeneracy in cell.And ubiquitous ligase enzyme is responsible for the poly tree is attached to predetermined protein to degrade, and ubiquitous protein stops the effective branch of the tree of growth.Is problematic based on the similarity with ubiquitous associated protein enzyme above-mentioned to the supposition that relates to the F40F12.5 function, does not detect so far whether particular proteins has ubiquitous polymeric enzymatic activity.A pair of in addition viewpoint can not make consistent:

A) it is believed that catalitic zone in the subclass of ubiquitous proteolytic enzyme is at F40F12.5 with clone and cannot not be conservative in 10;

B) except its catalytic site, the final demonstration of enzyme (from the bacterium to people) that derives from ubiquitous proteolytic enzyme family does not have sequence similarity, and the homology that F40F12.5 and clone 10 show to a certain degree.

Therefore, as if RAP-2 is specific RIP-conjugated protein and the therefore RIP active conditioning agent/mediation agent of encoding.Indirect influence is arranged and also be active conditioning agent/mediation agent in the RIP born of the same parents according to the conjugated protein confrontation RIP of its ability RAP-2 in conjunction with RAP-2.

Therefore, because RAP-2 is at adjusting/transmitting inflammation, cell survival and/or cell above activity obviously have effect, wherein RIP directly or indirectly especially participates in being caused or which relevant cytotoxicity and inflammation of inductive by various stimulants, described stimulant comprise by means of TNF/NGF receptor family and other possible acceptor shift which (for RIP participate in the scheme of incident in the born of the same parents and therefore RAP-2 participate in, referring to Fig. 1 of people such as Malinin, 1997).

RAP-2 also can be used as the inhibitor of Cytotoxic inhibitor and inflammation by means of the part with other proteinic mixture for example RIP that exists and the protein that is attached to RIP, it can influence these other protein (p55-R for example like this, FAS-R, MACH, Mch4, G1 and MORT-1) cytotoxicity or the effect of inflammation, finally cause its cytotoxicity or to the active inhibition of inflammation.

RAP-2 also can be used as cytotoxicity, inflammation add hadron or enhanser, and by strengthening other activity of proteins, RIP for example mentioned above and other protein that is attached to RIP, help to reclaim these protein, reclaim product and be used to strengthen the cytotoxicity of range protein or strengthen its inflammatory effects by RIP.

Similarly, the invention provides the relevant protein (RAP-2) of coding RIP, its abnormal shape, analogue or segmental dna sequence dna can be attached in RIP and adjusting or the mediation RIP fragment born of the same parents active, and activity is the adjusting/mediation of inflammatory and/or necrocytosis and/or cell survival in the described born of the same parents.

Particularly, the invention provides the dna sequence dna that is selected from following group:

(a) derive from the cDNA sequence of the natural proteinic coding region of RAP-2;

(b) under medium rigorous condition can with the sequence hybridization of (a) and encoding human learn active RAP-2 protein DNA sequence; With

(c) dna sequence dna and the encoding human of middle definition are learned active RAP-2 protein DNA sequence because the genetic code degeneracy is for (a) with (b).

Another specificity embodiment of the present invention's dna sequence dna mentioned above is to comprise the dna sequence dna that is encoding to the proteinic partial sequence of RAP-2 of an abnormal shape of small part to small part.Another embodiment of above-mentioned dna sequence dna is the proteinic sequence of coding RAP-2, as describing in Fig. 1.Also having another embodiment is the dna sequence dna that is shown in Fig. 2.

The invention provides its analogue of RAP-2 protein and any above-mentioned sequence encoding of the present invention, fragment or derivative can be attached to the biologic activity of RIP and adjusting/mediated cell death and/or cell survival approach.

Specificity embodiment of the present invention is a RAP-2 protein, its analogue, fragment or derivatives thereof.Be shown in Fig. 3 as RAP-2 protein sequence from Fig. 1 and Fig. 2 supposition.Another embodiment is the proteinic abnormal shape of any RAP-2, its analogue, fragment or derivative.

The present invention also provides the carrier that repeats to express that comprises above-mentioned DNA, these repeatably expression vector can be in suitable eucaryon or prokaryotic host cell expression vector; The eucaryon or the prokaryotic host cell that transform contain so repeatably expression vector; Provide and be suitable for described protein, analogue, produce RAP-2 protein of the present invention by such transformed host cell of growing under the condition that the fragment number derivative is expressed, or its analogue, the method of fragment or derivative, realize the described proteinic back modification of translating, as obtaining described protein from the substratum of described transformant or from the cell extract of described transformant and extracting described marking protein, analogue, fragment or derivative are needed, and above-mentioned definition is in conjunction with being used to comprise proteinic all abnormal shapes of RAP-2.

Another aspect, the present invention also provides specificity in the proteinic antibody of RAP-2 or reactive derivative or fragment and analogue of the present invention, fragment and derivative.

The present invention also has another aspect, and the various application of above-mentioned DNA or its encoded protein matter are provided, and its application comprises as described below according to the present invention:

(i) be used to regulate inflammation in the born of the same parents that regulate or mediate by protein RIP, the method of the adjusting of necrocytosis and/or cell survival approach, comprise with one or more and can be attached to RAP-2 protein, its abnormal shape, analogue, the described cell of fragment or derivatives for treatment, the treatment of wherein said cell comprises described one or more protein, its abnormal shape, analogue, fragment or derivative import to described cell in the mode that is suitable for importing in the born of the same parents, or with the suitable carriers of carrying described sequence with one or more protein, its abnormal shape, analogue, fragment or derivative import to described cell, suitable will effectively the working in the described cell of being inserted in of described sequence that described carrier can be expressed in described cell with described sequence.

(ii) according to above-mentioned (i), effect by means of rip protein, be used to regulate based on the effect of pair cell ligand-mediated inflammation by TNF family, the method of necrocytosis and/or cell survival approach, the treatment of wherein said cell comprises in the mode that is suitable for importing in the born of the same parents described RAP-2 protein, special-shaped, analogue, fragment or derivative import in the cell, or with the form of the suitable carriers that is suitable for the carrying described sequence described G1 protein of will encoding, or it is special-shaped, analogue, the dna sequence dna of fragment or derivative imports to described cell, and described carrier can realize that the form that described sequence is done to express at described cell with described sequence is inserted into described cell.

(iii) in above-mentioned method (ii), wherein, comprise step by treating described cell with the above-mentioned cell of recombinant animal virus vector transfection:

(a) make up the sequence and the surface of carrying coding expression surface protein (part) and be selected from RAP-2 protein, special-shaped, analogue, the recombinant animal virus vector of second sequence of fragment and derivative, described surface protein can be in conjunction with the specific cell surface receptor of the cell surface that carries FAS-R and p55-R, when in cell, expressing, can regulate/mediate inflammation in the born of the same parents, necrocytosis and/or cell survival approach; With

(b) infect described cell with (a) described carrier.

(iv) regulate inflammation by ligand-mediated being used to of TNF family by means of the effect of rip protein, the method of necrocytosis and/or cell survival, comprise with antibody of the present invention or active fragments or derivatives thereof and treat described cell, described treatment is that suitable composition is applied to described cell, said composition contains described antibody, the active fragments or derivatives thereof, wherein when contacting with born of the same parents' outside surface to small part RAP-2 protein, described composition is formulated as born of the same parents and uses outward, when described RAP-2 protein is born of the same parents planted agent's time spent fully, described composition is formulated as in the born of the same parents and uses.

(v) regulate inflammation by ligand-mediated being used to of TNF family by means of the effect of rip protein, the method of necrocytosis and/or cell survival, this method comprises with the oligonucleotide sequence to the antisense sequences of small part of the RAP-2 protein sequence of the present invention of encoding treats described cell, and described oligonucleotide sequence can stop the RAP-2 protein expression.

(vi), comprising as above-mentioned tumour cell or the cell of HIV infection or the method for other disease cell of (ii) being used for the treatment of:

(a) make up the sequence and the coding that carry coding virus surface proteins matter and be selected from RAP-2 protein of the present invention, its analogue, the recombinant animal virus vector of the proteinic sequence of fragment and derivative, described surface protein can be attached to specific tumor cell surface acceptor or the cell surface receptor of HIV infection or the acceptor that is carried by other disease cell, when expressing in described tumour, HIV infects or other disease cell can kill described cell by the effect of rip protein; With

(b) carrier of usefulness (a) infects cell or other disease cell of described tumour or HIV infection.

(vii) regulate inflammation by ligand-mediated being used to of TNF family by means of the effect of rip protein, the method of necrocytosis and/or cell survival, comprise and use the ribozyme step, wherein the surface can be imported to described cell in the mode that allows described ribozyme sequence to express with the carrier of the interactional ribozyme sequence of the coding proteinic cell mRNA sequence of RAP-2 of the present invention in described cell, express in described cell with wherein said ribozyme sequence, the mRNA sequence of it and described cell interacts and the described mRNA sequence of cracking causes the expression of described RAP-2 protein in described cell to be suppressed.

(the viii) method of from described method of the present invention, selecting, wherein said RAP-2 protein coding sequence comprise at least of the present invention can be in conjunction with the RAP-2 abnormal shape of RIP, its analogue, fragment and derivative.

(ix) separate and differentiate the method that can be attached to rip protein of the present invention, comprise two hybridization programs of using yeast, the sequence of described rip protein of wherein encoding is carried by a hybrid vector and the sequence that comes from cDNA or genome dna library is carried by second hybrid vector, then carrier is used for transformed yeast host cell and isolating positive transformant, is attached to proteinic sequence on the described rip protein by extracting described second hybrid vector to obtain coding subsequently.

(x) according to above-mentioned (i)-(x) each described method, wherein RAP-2 protein is the abnormal shape of RAP-2, analogue, one of fragment and derivative.

(xi) according to above-mentioned (i)-(x) each described method, wherein RAP-2 protein or its any abnormal shape, analogue, fragment or derivative participate in the adjusting by the effect of the cell of other mediation agent or inductor mediation, described RAP-2 protein, abnormal shape, analogue, two in fragment or derivative directly or indirectly are attached to mediation agent or inductor.

The present invention also provides and has been used to regulate inflammation, by means of the necrocytosis of the effect mediation of the effect of the effect TNF family pair cell of rip protein or aforesaid any other mediation agent or inductor pair cell and/or the pharmaceutical composition of cell survival approach, comprise one of any following as active ingredient:

(i) RAP-2 protein of the present invention and biological active fragment, analogue, the mixture of derivative;

(ii) coding can be in conjunction with the protein of cell surface receptor and the recombinant animal virus vector of coding RAP-2 protein of the present invention or biological active fragment or its analogue;

The following oligonucleotide of the following antisense of protein of the present invention of (iii) encoding is following, and wherein said oligonucleotide may be second sequence of above-mentioned recombinant animal virus vector (ii).

The present invention also provides:

I. be used for inflammation, by born of the same parents' inner cell death of rip protein adjusting/mediation and/or cell composition approach or other mediation agent or inductor, or the method for the adjusting of the effect of other NF-κ B inductor or inhibitor pair cell, comprise protein with RAP-2, its abnormal shape, analogue or fragment or with coding RAP-2 protein, special-shaped, analogue or its fragments sequence are according to the described cell of one of the method for above-mentioned (i)-(x) treatment, described treatment causes the reinforcement or the inhibition of the effect of described RIP mediation, thereby also strengthen or suppressed the effect of FAS-R or p55-R-mediation, or described other mediation agent or inductor, or the reinforcement or the inhibition of other NF-κ B inductor or inhibitor.

II. aforesaid method, wherein said RAP-2 protein, analogue, fragment or derivative are the proteinic parts of RAP-2, and it participates in being attached to RIP specifically, or described other inductor or mediation agent, or other NF-κ B inductor or inhibitor, or the proteinic part of described RAP-2 protein sequence coding RAP-2, it participates in the combination of RIP specifically, or described other mediation agent or inductor other NF-κ B inductor or inhibitor.

III. aforesaid method, wherein said RAP-2 protein is one of any RAP-2 abnormal shape, described abnormal shape can be strengthened the relevant effect of RIP-.

IV. aforesaid method, wherein said RAP-2 protein is one of any RAP-2 abnormal shape, described abnormal shape can suppress the relevant effect of RIP-, thereby or other or other mediation agent or induce, or the effect of other cytotoxicity mediation agent or inductor pair cell to the correlation of anti-cell and FAS-R-that also can suppress pair cell or the relevant effect of p55-R-.

V. aforesaid method, wherein said RAP-2 protein, abnormal shape, analogue, fragment or derivative can be by means of directly or indirectly suppressing NF-κ B or directly or indirectly activating JNK or the p38 kinases is strengthened or suppressed inflammation and cell survival approach.

Can adopt for example yeast crossbreeding method of the triage techniques that is used to separate and differentiates any standard of protein, the affinity chromatography method carries out with the standard program that those skilled in that art know that RAP-2 is proteinic to be separated, and identifies and qualitative.

In another aspect of the present invention, in two screening by hybridization of yeast with RAP-2 protein itself, or its abnormal shape, fragment or derivative make protein bound on it as bait.

Be attached to RAP-2, its abnormal shape, the protein of fragment or derivative also is a part of the present invention.

Also the invention with following detailed provides others of the present invention and embodiment.

Should be noted that, the following term of Shi Yonging in the text: " RIP; and FAS-part, or the adjusting/mediation of the effect of TNF pair cell " and any other " adjusting/mediation " of mentioning in specification sheets are believed to comprise external and intravital treatment, also comprise inhibition or reinforcement/increase in addition.

The accompanying drawing summary

Fig. 1 (A, B) (SEQ ID NO:1) shows the nucleotide sequence of RAP-2, under be scribed ss the initial sum terminator codon.It is initial that the 1.5Kb that the arrow indication is obtained by two screening by hybridization clones;

Fig. 2 (A, B) (SEQ ID NO:2) shows the nucleotide sequence of clone #41072 (referring to embodiment 1), under be scribed ss the initial sum terminator codon.

Fig. 3 A (/ 1, / 2) aminoacid sequence and the B (/ 1 of the supposition of the varient of demonstration people (20.4 total lengths and people shrt) and mouse (NEMO total length and mouse part) splicing RAP-2, / 2) show that utilization is at BCM Search Launcher (Baylor College of Medicine, Houston, TX) the disclosed sequence of the FIP-2 of obtainable software packaging box arrangement, in the box is homologous amino acid, and identical amino acid is gray shade.(B) star in is represented leucine-slide fastener (the LZ)-similar motif of the hypothesis among the FIP-2.

Fig. 4 has described the molecular characterization of RAP-2.In the Northern blot hybridization of the dna fragmentation of people MTN trace 1 (Clontech) and RAP-2, in B as be attached to the RAP-2 of RIP in the analysis that embodiment 3 describes in detail.The interaction of NIK-RAP-2 is as detecting in (B) in C, and different is that anti--FLAG antibody can be used for the Western trace, subsequently with anti--His6 immunoassay.Arrow is represented the proteinic position of immunoassay.

Fig. 5 expresses by the ectopic of the RAP-2 that describes among the embodiment 4, by the representative graph of the passive downward modulation of various stimulation activated NF-κ B and c-Jun.(for NF-κ B (A) is HIVLTR-Luc or CMV-Luc with the report plasmid, for c-Jun (B) active testing is GAL4-Luc), with the interim transfection HEK-293T cell of plasmid (being labeled as pcRAP-2-in the accompanying drawings) for the expression vector and the empty carrier (only being labeled as pcDNA3 in the accompanying drawings) of the inductor of indicating or the total length RAP-2 that encodes, the activation of expressing gene luciferase is represented with relative luciferase unit (R.L.U.).

Fig. 6 is illustrated in the interior RAP-2 of wide concentration range NF-κ B and c-Jun is shown similar inhibition behavior.PcRAP-2 of the amount of TRAF2 and various indications (justice is arranged) or pcRAP-2-a/s (antisense) construct are expressed in the HEK-293T cell temporarily.In order to estimate the activation of NF-κ B (A) and c-Jun (B), induce pHIVLTR-Luc and pGAL4-Luc report plasmid respectively.Fig. 5 of embodiment 4 has described the test of luciferase.

Fig. 7 shows that RAP-2 strengthens the phosphorylation of the c-Jun of signal induction powerfully, does not disturb the activation level of JNK1/2.

(A) phosphorus-Jun antibody that adopts Western engram analysis method to describe with embodiment 5 is differentiated with the expression construct of indication with in the accompanying drawings by the pcRAP-2 that is represented by plus sige (+) in the pcDNA3-carrier of negative mark (-) expression and the accompanying drawing total cell pyrolysis liquid of HEK-293T cell of transfection together, the control film that shows on lower swimming lane is with resisting total c-Jun Abs (NEB) pre-detection

(B) Abs of the anti-phosphorus-JNK that describes in detail with embodiment 5 carries out the Western engram analysis to total lysate, detect come from pcDNA3 or pcRAP-2 transfection and with hrTNF α treatment so that the activatory JNK1/2 of the HEK-293T cell of rise time.

(C) with HA-JNK1 expression plasmid and empty carrier, the HEK-293T cell of the various combination cotransfections of pcRAP-2 and pcRIP carries out immunoassay by means of the terminal HA-label of its N-, measures the ability of the GST-Jun of bacterium phosphorylation purifying in the vitro kinase test.By SDS-PAGE analytical reaction product.By arrow mark GST-Jun.

Fig. 8 shows that RAP-2 is not attached to DNA with NF-κ B and AP-1 competition.With the protein (-) of independent indication or with pcRAP-2 (+) transfection HEK-293T.To cultivate altogether from the nuclear extract of cell preparation and the oligonucleotide of 32P mark, described oligonucleotide comprises the recognition sequence to the classics of AP-1 (A) or NF-κ B (B).PAGE analytical reaction product by non-sex change.

Fig. 9 shows the RAP-2 influence basal level with the NF-κ B of the HEK-293T of the RAP-2 (justice is arranged) of variable quantity or the interim transfection of RAP-2-antisense (a/s) and HeLa cell.The all operations of Fig. 6 description carrying out as embodiment 4.

(A, B) (SEQ ID NO:3) shows the partial nucleotide sequence of clone #10 to Figure 10.

Figure 11 shows the functional performance of the RAP-2 of serial disappearance.In A, the successive C-terminal deletion of diagram RAP-2, all clipped forms are shared complete RAP-2N-end, and their C-end is represented by arrow.Under be scribed ss RIP, NIK, IKK β and TIP60 calmodulin binding domain CaM.Three hatch square frames are corresponding with the similar motif of the leucine-slide fastener of supposition.B shows the HIV-LTR luciferase report plasmid utilize NF-κ B, and the overexpression of the disappearance construct of describing in A is to by RelA, and TRAF2 TNF and NIK are to the effect of the NF-kB activation of HEK-293T cell.The active activation of reporter gene luciferase is represented with relative luciferase unit (R.L.U.).

Figure 12 shows the physical structure figure of RAP-2 function and calmodulin binding domain CaM.

(A) ability of the combination of proteins of the yeast (odd column) of the RAP-2 of the various disappearances of test and transfection and the indication in the Mammals HEK-293T cell (even column).Two rightmost row be presented at as embodiment 9 describe with a large amount with the ability of identical disappearance transfection, to suppress the NF-kB activation and to start the c-Jun hyperphosphorylation (c-Jun) that treatment is replied to TNF-α to HEK-293T.The intensity of boldness of intersecting and given effect is proportional.The construct of star expressive notation is different [referring to Figure 11 (B)] to the observed effect that Rel-A stimulates.

(B) representative infers that from deletion analysis the regional position display in the combination (top) of RAP-2 and functional (bottom) in (A), only arranges proteinic skeleton.Hatch part is indicated the possible position on the border of corresponding elementary zone.

Figure 13 shows that the ser-148 of RAP-2 is necessary for the c-Jun hyperphosphorylation of inducing ser-63.

Shown the Western trace, wherein wt is meant wild-type, and S148A is meant that 148 ser is substituted by L-Ala and this carrier is empty control vector.

Detailed Description Of The Invention

The present invention relates to new protein RAP-2 on the one hand, it can be attached to the RIP egg White matter, thus can specificity mediation or the ratio activity of regulating RIP. And RIP participates in The inflammation of above-detailed, adjusting or Jie of cell death and/or cell survival approach Lead. Therefore RAP-2 can strengthen inflammation, cell death and/or cell survival approach The RIP activity maybe can be strengthened the RIP activity of one of these approach, and press down on the other hand Make it.

More particularly, according to the present invention, provide new protein RAP-2. Through RAP-2 being checked order with qualitative, find that RAP-2 is the height spy who has RIP The RIP-conjugated protein of the opposite sex, but do not have in demonstration and the many known participation cells The combination of the protein of signal formation approach causes producing inflammation, cell death or thin Born of the same parents' survival. RAP-2 does not obviously have with the activated protein of tool in these approach yet Common zone, namely RAP-2 does not have " death domain " motif or module, and it does not have Kinases motif or zone and do not have protease zone or a motif. The RAP-that measures 2 sequences also are unique sequences, as from comprising Genebank with many databases, people's base Because of group level 1, the sequence that obtains in ' dbest ' database relatively. Retouch in detail as mentioned (also with reference to all publications and the aforesaid patent application) RIP that states participates in the cell Inflammation, cell death and cell survival approach. Therefore, the adjusting of RIP activity or control System can be regulated one of these approach or all approach, when by for example with TNF or When being attached to its acceptor, FasL starts such approach (particularly TNF, p55-R). RIP can be crucial at utmost playing a part at this pathway activation of mensuration, by means of It is in conjunction with many ability and also combinations with Cytotoxic protein of death domain Many abilities with kinase activity. So protein of the present invention, for example specificity Be attached to RIP RAP-2 protein may in regulating the RIP activity, play important Act on, thereby compare the degree of inducing an approach that is adjusted to other. Therefore. this The interior conditioning agent of cell or mediation agent that the RAP-2 protein representative of invention is important.

Except RAP-2 full length protein of the present invention, will than short cDNA clone, send out Now be the sequence " obstruction " that origin comes from " total length " cDNA zone of several edge far away, Obviously produce the splicing of homologous genes. Differentiate people RAP-2's by research ESTs set The corresponding body of mouse.

RIP-RAP-2 mutually in the HEK-293T that has further confirmed transfection and the HeLa cell The physiology correlation of mutual effect. But such complex formation does not cause the RIP enzyme Short active, there is not phosphorylation RAP-2 to prove such as the RIP by overexpression.

Transfection experiment in mammal HEK-293T cell also causes RAP-2-NIK The stable formation of compound.

RAP-2 is the key element of NF-κ B and c-Jun signal transduction pathway seemingly, by Be attached to NIK in it, IKK β and TIP60 (histone acetyltransferase) and adjusting NF-κ B With the c-Jun dependent transcription. In fact, the expression of the RAP-2 dystopy of reinforcement cause right The inhibition that NF-κ B replys causes adding and lack from cell by means of antisense constructs Strong NF-κ B and c-Jun trans-activation.

Find that also RAP-2 starts the c-Jun hyperphosphorylation, is not situated between by the activity of JNK Lead. RAP-2 does not suppress c-Jun and RelA is attached to DNA. By deletion analysis successively Differentiated combination and the functional region of RAP-2, these researchs have indicated RIP, NIK Overlapping and find in the amino acid 95-264 of RAP-2 with the calmodulin binding domain CaM of TIP60. But the downstream function of finding to be mediated by RAP-2 is with the N-end region with protein The territory comprises amino acid/11-264 location.

According to above-mentioned RAP-2 seemingly the stress signal of replying network weaken determining of circuit Element qualitatively: there is the expression inhibiting of dystopy of the construct of justice coding to reply, and anti-The expression booster response of justice coding construct. In fact, in inventor's laboratory also Known RAP-2 is that RAT (RIP ' that weakens s), and therefore thinks RAT in this article And/or RAT-303 and/or clone 303.

The existence indication of a plurality of variants is at least partially in RAP-under the given condition As if 2 final effect depends on that sequence blocks the existence of piece, and it is for general different Combination/the target of the protein of type hits/transduces/and to modify be necessary. If for example with RAP-2 are attached to TIP60, allow the location of the former nuclear, suppose to have the position of appraising and deciding of splicing The RAP-2 variant of (NLS) of signal can be defective in the inhibition of NF-κ B/AP-1 Or on the contrary exceedingly activation. Sequence analysis shows that RAP-2 carries the big of known NLSs Several bunches of (E, K and R) characteristics of most positive electric charges.

Made up the physical map of the RAP-2 that is attached to RIP to the RAP-2 zone. on The protein of stating originates in 177-218 amino acid and terminal at 264. In the RAP-2 The RIP calmodulin binding domain CaM is not overlapping with the NIK binding site with IKK β yet.

Be attached to TIP60, the family of many nucleoproteins is referred to as the histone acyl group and shifts Enzyme, obviously this collection of illustrative plates is in this regional cross amino acid 95-264. Discovery participation homology-Dimeric zone location is between amino acid 217-264.

The data of accumulation hints function affect (the called after NF-kB of all RAP-2 Inhibition and induce the c-Jun hyperphosphorylation) collection of illustrative plates be same area.

Protein by clone #10 coding is obviously initial between amino acid 218-309 And combination in 416 zones of amino acid, thus its binding site can comprise with RIP, NIK, the overlapping region of IKK β and TIP60 binding site.

In addition, the zone location that is formed in conditioning signal effectively by all derivants foot N-end segments to this protein.

There is effect in the zone that is comprised by amino acid 95-416, although it obviously a little less than, with The comparison of situation about being caused by full length protein is therefore by the reinforcement of endogenous RAP-2 Polymerization produce.

In addition, except RelA, all effects of inducing in our experiment are by little To the mediation of the-terminal amino acid of 100 RAP-2, in fact comprise 1-102 ammonia Although the different effect of fragment mediation of base acid is quite gentle.

On the other hand, the inhibition of the effect of ReIA-mediation needs longer part RAP-2. Up to now, we have defined the border in amino acid/11-264 zone, The zone that it is obviously granted between amino acid/11 57 and 264 has some specificitys, RelA-Relevant binding characteristic.

According to top viewpoint, as if:

A. except ReIA, RAP-2 is in conjunction with RIP, clone #10 and most possible NIK and TIP60 does not need for the function of this protein, the NF-κ B's that induces such as overexpression Inhibitor.

B. the obvious at least part of quilt of effect of RAP-2 activation that the RelA overexpression is induced Different binding events mediations basically, finds that protein above-mentioned helps Given activity is as inferring from the experiment of carrying out at present.

Because FAS-R and TNF acceptor cause the ability of dead uniqueness, and TNF is subjected to Body is attacked the ability of various other tissues damage activity, these function of receptors unusually right Organism is especially harmful. Really, the excessive and defective function of verified these acceptors Help the physiology performance of various diseases. Participate in the signal formation activity of these acceptors Molecule discriminating and regulate the discovery of mode of the function of these molecules, it is right to have consisted of The potential clue of the new treatment approach of these diseases. Consider RIP FAS-R and Existence doubtful in the p55-R toxicity important function, therefore by means of the adjusting RAP-of RIP The 2 couples of FAS-R and TNF existence doubtful are in important regulating action, and design is RAP-therein 2 help to strengthen under the Cytotoxic condition of RIP mediation, by means of stoping RAP-2 Be attached to RIP or suppress RAP-2 and RIP between interaction can stop the poison of RIP The medicine of sexual function (as mentioned above RIP to itself and with have other of death domain Protein has cytotoxicity).

Equally, also known (as mentioned above) FAS-R and p55-R participate in the activation of NF-κ B, Thereby and the activation of participation cell survival. Therefore, when the needs cell killing, example Such as cancer cell, the cell that HIV infects etc., the cell toxicant of reinforcement FAS-R and p55-R The property effect be gratifying (protein relevant with them is MORT-1 for example, MACH, Mch4, G1, TRADD), and induce NF-κ B at known its of same time Ability. Therefore, interact or strengthening NF-κ B in conjunction with causing as RAP-2 and RIP Induce in strengthen the possible effect of RIP (by means of TRAF2 with by means of the kinases district The intermediate zone of territory and/or RIP), stop then mutual work between RAP-2 and the RIP In order to inhibition, or the enhancing that stops at least NF-κ B to activate, thereby TNF-or FAS-shifted Part-effect of inducing and the balance of Cytotoxic side increase farthest to provide The cell death that adds.

Similarly, for (opposite with situation mentioned above) in the opposite situation, RAP-2 In fact cause FAS-R and p55-R inflammation or cytotoxic effect with the activation of RIP Inhibition, for example suppress, various autoimmune diseases etc. are when thinking the cell that increases Survival, the interaction between design reinforcement RAP-2 and the RIP is to strengthen cell then Balance between dead overall inhibition and the transitional cell survival. Also mention above the basis RAP-2 ' s and the interaction of RIP cause strengthening the RIP ' s merit of NF-κ B in activating The inhibition of energy when the needs cell survival, stops the mutual work of RAP-2 and RIP then With, thereby the RIP ' s activity of strengthening in the NF-κ B activation is necessary.

Consider mentioned abovely, it has produced RIP in inflammation, and cell death or cell are deposited Balance between the inducing or mediate of the approach of living has crucial effect, so RAP-2 Because the conditioning agent that is RIP has the important function that is equal to. Utilize upper and lower literary composition to mention Various medicines or treatment affect RAP-2-RIP interaction/combination, can allow by carefully Signal transduction pathway in the born of the same parents cell transfer of checkmating becomes living cells, and vice versa.

RAP-2 protein DNA sequence and by this DNA order the present invention also relates to encode The RAP-2 protein of row coding.

In addition, the invention further relates to the BA of coding RAP-2 protein Analog, fragment and derivative, the dna sequence dna of its analog and derivative. Participate in Standard technique can prepare such analog, fragment and derivative (referring to for example, The people such as Sambrook, 1989), wherein can lack stack or by another codon Substitute the one or more codons in the coding RAP-2 protein DNA sequence, with Generation has to compare with native protein at least and has amino acid residue and change.

The RAP-2 protein that can compile, abnormal shape, analog, fragment or derivative upper Stating that dna sequence dna comprises can be with the code area that derives from natural RAP-2 protein The DNA of cDNA hybridization, wherein such hybridization be moderately, strictly under the condition The RAP-2 protein of dna sequence encoding BA that carry out and interfertile. Therefore the dna sequence dna of these hybridization comprises with natural RAP-2 cDNA sequence having height The homology of degree has represented the similar sequence of RAP-2, for example can be that coding is various The natural sequence of deriving of RAP-2 abnormal shape, or coding belongs to one group of similar order of RAP-2 The natural sequence that exists of the protein with RAP-2 activity of row coding. Further, For example these sequences also can comprise what non-natural existed, the synthetic sequence that produces, it Similar with natural RAP-2 cDNA sequence, but comprise the modification of many needs. Such composition sequence comprise all possible coding RAP-2 analog, fragment and The sequence of derivative, all these all have the RAP-2 activity.

In order to obtain the similar sequence of naturally occurring RAP-2 recited above, can Utilize natural RAP-2 cDNA or its part as probe screening with separate come from various The natural derived dna of tissue or the standardization program of RNA sample (referring to Sambrook etc. The people, 1989 standardization programs of listing).

Equally, in order to prepare the analog of coding above-mentioned RAP-2, fragment or The various synthetic similar sequence of RAP-2 of derivative can be used hereinafter and retouch in detail The many standardization programs about the preparation of analog, fragment and derivative of stating.

The polypeptide or the protein that " correspond essentially to " RAP-2 protein not only comprise RAP-2 protein and comprise it being polypeptide or the protein of RAP-2 analog.

The polypeptide that corresponds essentially to RAP-2 protein is those polypeptides, one of them Or the amino acid of a plurality of RAP-2 protein is removed by another amino acid replacement And/or insert, condition is that the protein that obtains is gone up the demonstration RAP-2 corresponding with it substantially Protein is identical or higher BA arranged.

In order to correspond essentially to RAP-2 protein, the sequence of common RAP-2 protein In variation for example abnormal shape is relatively less. Although the amount that changes can be more than 10, preferably No more than 10 variations in ground, more preferably no more than 5 variations are most preferably no more than Three such variations correspond essentially to RAP-2 when any technology is used for seeking The potential biologically active proteins matter of protein, a kind of such technology is to be applied in The induced-mutation technique of the routine on the coded protein DNA causes producing several modifications. Sieve Select the protein of such clonal expression to be attached to RIP upward and to regulate aforesaid RIP is to regulating/mediate the ability of the activity of approach in the born of the same parents.

" guarding " variation is to expect to change the active of protein and usually first Earlier screened those variations of arriving are because expect that these variations can not change this basically The size of protein, electric charge or configuration, therefore expection can not change its biological characteristics.

The conservative alternative analog that comprises of RAP-2 protein, wherein polypeptide at least An amino acid residue has conservatively been substituted by a different amino acid. Preferably Ground adopts normal experiment to measure according to following such substituting of listing at Table I A Like this substitute synthetic peptide molecule with the 26S Proteasome Structure and Function characteristic that modification is provided, And the BA of the protein of maintenance RAP-2.

Table I A

Original residue typically substitutes

Ala Gly；Ser

Arg Lys

Asn Gln；His

Asp Glu

Cys Ser

Gln Asn

Glu Asp

Gly Ala；Pro

His Asn；Gln

Ile Leu；Val

Leu Ile；Val

Lys Arg；Gln；Glu

Met Leu；Tyr；Ile

Phe Met；Leu；Tyr

Ser Thr

Thr Ser

Trp Tyr

Tyr Trp；Phe

Val Ile；Leu

Perhaps, the alternative of another group of RAP-2 protein is wherein at least to remove In the polypeptide amino acid residue and insert in its position according to following table 1B Different residues. The type that substitutes for preparing in polypeptide can be based on different kinds Homologous protein matter between the analysis of the frequency that changes of amino acid, Schulz for example Deng the people, G.E., the protein structure principle, Springer-Verlag, NewYork, NY, 1798, and Creighton, Fig. 3 to Fig. 9 of T.E.: structure and molecular characterization, W.H.Freeman ﹠ Co., San Francisco lists among the table 1-2 of CA 1983 Those. Based on such analysis, below the alternative definitions that this paper is conservative with another kind is One of 5 groups in exchange:

Table I B

1. little is aliphatic, the nonpolar or residue of polarity: Ala a little, and Ser, Thr (Pro, Gly);

2. the electronegative residue of polarity and its amide: Asp, Asn, Glu, Gln;

3. polarity, the residue of positively charged: His, Arg, Lys;

4. big aliphatic nonpolar residue: Met, Leu, Ile, Val (Cys); With

5. the residue of big fragrance: Phe, Tyr, Trp.

Three amino acid residues in the above-mentioned bracket have in the architecture of protein Specific effect. Gly is unique residue that loses side chain and therefore gives the chain spirit Active. But this trends towards promoting the formation of second structure rather than a-spiral helicine. Because its unusual geometry, so can clamp tightly this chain and usually trend towards Cys promotes β-circle-similar structure, although can participate in disulfide bond in some cases Formation, it is important for the folding of protein. Note the above people such as

Schulz Merging group

1 and 2. Be further noted that since Tyr in conjunction with the potentiality of hydrogen, so itself and Ser and Thr Deng having obvious kinship.

The known for example conservative ammonia of the present invention recited above of those skilled in that art Substituting of base acid, and be expected at the biology that amino acid replacement keeps this polypeptide afterwards With structural characteristic. Most disappearance of the present invention and to substitute be that those are at albumen Characteristic in matter or the peptide molecule does not produce the variation of group. " characteristic " defined For the mode with non-removing property changes second structure, for example change of a-spiral or β-sheet Change, and the variation in BA, for example be attached to Jie of RIP and/or RIP Lead the impact to cell death.

In protein, produce the example of amino acid replacement, can be used for obtaining the present invention The analog of RAP-2 protein, the step of the method is known, for example the U.S. The people's such as patent Mark RE 33,653,4,959,314,4,588,585 and 4,737,462; The people's such as Koths 5,116,943; The people's such as Namen 4,965,195; The people's such as Chong 4,879,111; With the people such as Lee 5,017,691 in list with the U.S. the 4th, 904,584 The protein that the lysine of listing in number patent people such as () Shaw substitutes.

In addition, conservative substitute discussed above can not obviously change RAP-2 protein Activity, that no matter guards substitutes or less conservative and more change at random, All can cause the BA of the analog of RAP-2 protein to increase.

When confirm substituting or during the accurate effect of disappearance, it will be appreciated by those skilled in the art that combination by routine and necrocytosis test can estimate alternative, the effect of disappearance etc.Utilize such standard testing screening can not relate to too much experiment.

Acceptable RAP-2 analogue is the analogue that keeps the ability that is attached to RIP at least,, mediates the analogue of RIP ability in the approach in cell as mentioned above that is.By this way, can produce analogue with so-called main negative interaction, be referred to as not can be incorporated into RIP or subsequently signal form or in conjunction with after other active defective.For example such analogue can be used to suppress the effect of RIP, or suppress NF-κ B induce (directly or indirectly) of RIP acted on, this depends on that these activity are (referring to above) of the interaction conversion by RAP-2 and RIP, and by the combine competition of such analogue with natural RAP-2 with RIP.

On hereditary level, normally the site-specific mutagenesis preparation by the Nucleotide in coding RAP-2 protein DNA of these analogues, thereby produce the DNA of this analogue of coding, and afterwards synthetic DNA and in the reconstitution cell culture express polypeptide.Usually this analogue shows good biologic activity identical with naturally occurring protein or that increase, people such as Ausubel, the scheme that molecular biology is present, Greene press and Wiley Interscience, NewYork, NY, 1987-1995; People such as Sambrook, molecular cloning: laboratory manual, cold spring harbor laboratory, cold spring port, NY, 1989.

The proteinic preparation of RAP-2 of the present invention, or the alternative nucleotide sequence of coding phase homopolypeptide, be different from natural sequence, because the known degeneracy permission of genetic code changes, the site-specific mutagenesis of the analogue that sequence of the present invention can early prepare by encoding or the RAP-2 protein DNA of natural form obtains.Site-specific mutagenesis allows the specific nucleotide sequence by the dna sequence dna that utilizes the mutant that coding needs, and the Nucleotide of the adjacency of q.s prepares this analogue, with the sequence of primer that enough sizes are provided and the complementarity of sequence, form stable duplex with both sides in the point of crossing of cross-section disappearance.Usually, preferred primer length is 20 to 25 Nucleotide, and each side of reformed sequence has 5 to 10 complementary Nucleotide.Usually, site-specific mutagenesis is that those skilled in that art are known, and as people such as Adelman, DNA2:183 (1983) publication exemplifies, and its disclosed content is incorporated herein by reference.

Will recognize that the phage vector that common site-specific mutagenesis technology utilization exists with strand and double chain form.The typical carrier that is used for site-specific mutagenesis comprises for example M13 phage vector, for example disclosed by people such as Messing, Cleveland is about the annual meeting of macromole and recombinant DNA for the third time, editor A.Walton, Elsevier, Amsterdam (1981), it openly for example is incorporated herein by reference.These phages are easy to obtain by commercial sources, and its purposes is that those skilled in that art are known usually.Perhaps, can use the plasmid vector that contains the single stranded phage initial point that duplicates people such as (, Enzymology method 153:3,1987) Veira to obtain single stranded DNA.

Site-specific mutagenesis described herein is by following described acquisition: the single-stranded vector that at first obtains to comprise in its sequence the dna sequence dna of relevant polypeptide.The oligonucleotide that carries the sequence of the sudden change that needs prepares by automatic DNA oligonucleotide is synthetic.Then with of the carrier annealing of these primers with single chain protein matter-sequence-contain sequence, and with archaeal dna polymerase for example telex machine polysaccharase I Klenow fragment contact, finish synthesizing of the chain that carries sudden change.Therefore the sequence of sudden change and second chain carry the sudden change that needs.Then this allos duplex is used to transform suitable cell, for example intestinal bacteria JM101 cell and selection comprise the recombinant vectors of the arrangement of the sequence of carrying sudden change:

After selecting such clone, can remove the RAP-2 protein sequence of sudden change and place suitable carriers, can be used for the transfer or the expression vector of the type of transfection appropriate host usually.

Therefore, use known DNA or RNA amplification technique, for example PCR and chemical oligonucleotide synthetic also can be external and/or body in detect, obtain and/or modify proteinic gene or the Nucleotide of coding RAP-2.PCR allows by multiple dna polymerase reaction amplification (number increase) specific dna sequence dna.This reaction can be used as substituting of clone; All these are that the understanding nucleotide sequence is needed.In order to implement PCR, design and the sequence complementary primer that needs.Then by synthetic this primer that produces of automatic DNA.Owing to can design primer to hybridize to any part of this gene, create conditions so that can stand the right mispairing of complementary base.The amplification in the zone of these mispairing causes the synthetic of mutagenesis product, causes the generation (being site-specific mutagenesis) of the peptide with new characteristic.Also, see above the 16th chapter referring to Ausubel.Also the synthetic reversed transcriptive enzyme that utilizes by coupling complementary DNA (cDNA) carries out PCR, with the synthetic parent material that RNA is used as the extracellular region territory of synthetic prolactin acceptor, does not clone.

In addition, design PCR primer to be to mix new restriction site or other characteristic, for example in the terminator codon of gene fragment end to be amplified.Alternative permission coding RAP-2 protein or its segmental gene order of the restriction site of 5 ' and 3 ' end of the gene order of amplification, custom is used for other sequence and/or the cloning site in abutting connection with carrier.

Other method of PCR and RNA and/or DNA cloning is that those skilled in that art are known, and can be used for the present invention based on instruction and the guidance of this paper, does not need too much experiment.The known method of DNA or RNA amplification includes but not limited to that polymerase chain reaction (PCR) and relevant amplification procedure are (referring to people's such as for example United States Patent (USP) Mullis 4,683,195,4,683,202,4,800,159,4,965,188; People's such as Tabor 4,795,699 and 4,921,794; 5,142,033 of Innis; People such as Wilson 5,122,464; People such as Innis 5,091,310; People's such as Gyllensten 5,066,584; People's such as Gelfand 4,889,818; People's such as Silver 4,994,370; People such as Biswas 4,766,067; 4,656,134 of Ringold; The PCR scheme: the guidance of methods and applications) and the sense-rna that utilizes target sequence carry out the amplification (the 5th, 130, No. 238 patents of people's such as Malek the U.S., commodity are called NASBA) of RNA mediation as double-stranded DNA synthetic template; With with people such as the use of DNA cloning and antibody labeling bonded trade PCR[Ruzicka, science 260:487 (1993); People such as Sano, science 258:120 (1992); People such as Sano, biotechnology 9:1378 (1991)], all patent documentation and publications all are incorporated herein by reference.

In a similar fashion, prepare the proteinic biology chemistry of RAP-2 fragment (for example any RAP-2 or its abnormal shape) with reference to the proteinic analogue of aforesaid RAP-2.The proteinic suitable fragment of RAP-2 is those biologic activity or other and direct or indirect other the relevant protein of RIP of having kept the ability of RAP-2 and can having regulated or mediate RIP, therefore, with reference to aforesaid analogue, preparation have the negative value of dominance or dominance on the occasion of the RAP-2 protein fragments of effect.Should be noted that these fragments represent the analogue of the present invention of specific type, be referred to as with they be defined as derive from total length RAP-2 protein sequence the proteinic part of RAP-2 (for example, come from any RAP-2 or its abnormal shape), part that each is such or fragment have the activity of any needs recited above.Such fragment can be a peptide.

Similarly, employing is to RAP-2 protein, its analogue or fragment or by in conjunction with RAP-2 protein, and its analogue or fragment are to another or molecule antibody for example, enzyme, acceptor can prepare derivative like the modification of the standard of the known one or more side groups of those skilled in that art.Therefore adopt those skilled in that art's known means as used herein " derivative " covered can be from the derivative of functional groups preparation, these groups are present in the side chain of residue or C-end or N-end group and comprise within the scope of the invention.This derivative can be for example carbohydrate or a phosphoric acid residue of Chemical Composition, and condition is that such component has identical with RAP-2 protein or higher biologic activity.

For example; derivative can comprise the aliphatic ester of carboxyl; can with the acid amides of the carboxyl of ammonia or one-level or secondary amine reaction; the free amino (for example, isocyclic aroyl group behind the alkanoyl) of N-acyl derivative that forms with the acyl group composition or the amino-acid residue that forms by acyl moiety or the O-acyl derivative (for example those of seryl or threonyl residue) of free hydroxyl.

Term " derivative " plan only comprises can not being those derivatives of 20 common natural amino acids that exist with an amino acid change.

RAP-2 is that protein or polypeptide are the sequence of amino-acid residue.The proteinic polypeptide of sequence of whole RAP-2 that this paper defines that comprises that plan will constitute big sequence is included in the scope of such polypeptide, as long as stack does not influence amino acid whose new features of the present invention, that is, if they keep or increase the proteinic biologic activity of RAP-2 or can be exemplified protein or the polypeptide that has the proteinic biologic activity of RAP-2 with remaining.Therefore, for example plan will the present invention includes the amino acid with other or the proteinic fused protein of RAP-2 of polypeptide.

New RAP-2 protein, its analogue, fragment and its derivative have many possible application, for example:

(i) in aforesaid inflammation, can be in necrocytosis or the cell survival with RAP-2 protein, its analogue, fragment and derivative are used to regulate the function of RIP.For example, if RAP-2 can regulate RIP ' s to NF-κ B, JNK (Jun kinases) or the kinase whose activatory effect of p38, when antitumor, resist or former inflammation, the application of anti-HIV is gratifying, and such RAP-2 effect causes strengthening the effect of such RAP-2-RIP.In some cases, the program of the known standard of employing itself can be strengthened cytotoxic effect with regulating inflammation, or stops the RAP-2 protein of cell survival effect, its analogue, and fragment or derivative import to cell.For example, when RAP-2 protein is (as suspecting) and only should import in the cell fully in the born of the same parents, and be gratifying by the FAS-R part of RIP mediation or the effect of TNF or other cytotoxic protein matter, the system that is used for this protein specific is imported to cell is necessary.A kind of mode is by preparation recombinant animal virus, for example derive from the virus of cowpox, two genes below wherein having imported, coding is attached to specifically the gene by the part of the cell surface proteins of this cell expressing, AIDs (HIV) virus protein gp120 for example, be attached to this protein specific some cell (CD4 lymphocyte and relevant leukemia), perhaps be attached to other part of the cell that carries FAS-R or p55-R specifically, described cell is the cell that carries FAS-R or p55-R; With the proteinic gene of coding RAP-2.The cell surface conjugated protein of therefore expressing on virus will target hits specificity and carries the virus of the cell of FAS-R-or p55-R in tumour cell or other, the RAP-2 encoding sequence is being imported to cell by means of virus and in case will cause FAS-R part that RIP mediates or the reinforcement of TNF effect or dependency RIP after expressing in cell.The recombinant animal virus (referring to people such as for example Sambrook, 1989) that the program construction of employing standard is such.Another kind may be the proteinic sequence of RAP-2 (for example, merging a kind of RAP-2 or its abnormal shape) that imports the oligonucleotide form, and described Nucleotide can and be expressed by cell absorption.

(ii) they can be used to suppress FAS-R part or TNF or relevant proteinic effect or the independently effect of RIP by the RIP mediation, for example, be similar in sapremic shock, transplant-right-host's repulsion, or in the acute hepatitis under the situation of tissue injury, wherein stop FAS-R part or TNF inductive FAS-R or p55-R intracellular signal to form or independently RIP effect, or the formation of the signal of other protein mediation is gratifying with increasing the cell survival approach simultaneously.In this case, for example adopt standard program, it is possible that oligonucleotide with the proteinic antisense encoding sequence of RAP-2 imports in the cell, thereby this will stop translating of the proteinic mRNAs of coding RAP-2 effectively and stop its expression and cause FAS-R part-or TNF-or RIP or other proteinic effect.Utilize above-mentioned recombinant virus approach by being that second sequence that the virus of oligonucleotide sequence is carried can import to cell with such oligonucleotide.

Equally, as mentioned above, based on the interactional characteristic of RAP-2-RIP, by above-mentioned (i) and method (ii), the approach of reinforcement or inhibition cellular inflammation and survival is possible.

Another possibility is to be used to be specific to the proteinic antibody of RAP-2 to form activity with signal in the inhibition cell.

The ribozyme method of development is that effect or the RIP that the another kind of RIP of inhibition mediates independently acts on recently.Ribozyme is the catalyzed RNA molecule of cleaving rna s specifically.Ribozyme can be carried out the target RNAs that genetically engineered is selected with cracking, the proteinic mRNAs of RAP-2 of the present invention for example encodes.It is competent in the sequence of RAP-2 protein mRNA with after by cracking mRNA or interact (complementary combination) that such ribozyme has specificity, causes the reduction of RAP-2 protein expression, according to target cell ribozyme expression levels.For the cell that ribozyme imported to selection (for example, carry those of FAS-R or p55-R), can use suitable carriers, for example, plasmid, animal virus (retrovirus) carrier, these carriers can be used for this purpose [also referring to top (i), wherein having the cDNA of the ribozyme sequence of coding selection as the virus of second sequence] usually.(comment, the method etc. that relates to ribozyme be referring to people such as Chen, and 1992; Zhao and Pick, 1993; People such as Shore, 1993; Joseph and Burke, 1993; Shimayama, 1993; People such as Cantor, 1993; Barinaga, 1993; People such as Crisell, 1993 and people such as Koizumi, 1993).This approach is suitable, because this RAP-2-RIP interaction is strengthened stoping cytotoxicity or worked as RAP-2-RIP interaction inhibition NF-kB activity is gratifying situation, is gratifying stoping this inhibitions to increase that such NF-κ B activates, promptly increase above-mentioned (ii) in cell survival be under the gratifying same case.

(iii) with RAP-2 protein, its analogue, fragment or derivative are used to participate in other proteinic separation of the identical category of intracellular signal forming process, differentiate and the clone, promptly be attached to RIP or be attached to functional relevant acceptor or proteinic those, in the application that can be used for two crossing systems of yeast recited above or after PCR clone, can be used for the system that the Southern of the non-strictness of use of development recently hybridizes people such as (, 1989) Wilks.In people such as Wilks open, described based on known kinases motif, after the kinase sequence of design, by differentiate and clone the protein-Tyrosylprotein kinase of two suppositions after the PCR clone by the application of the Southern hybridization of non-strictness.This approach can be used for utilizing the proteinic sequence of RAP-2 to be used to differentiate according to the present invention and cloning these relevant RIP bonded protein.

(iv) will utilize RAP-2 protein, or its analogue, the another kind of approach of fragment or derivative is used for the affinity chromatography method, can be in conjunction with for example other participates in the protein of intracellular signal forming process or other protein or the factor of the factor to separate and to differentiate.In this application, can be with RAP-2 protein of the present invention, its analogue, the single affinity chromatography matrices that is attached to of fragment or derivative causes and the contacting of cell extract then, or separates and suspect the protein or the factor that participates in the intracellular signal forming process.After the affinity chromatography program, can wash-out, separate and qualitative RAP-2 protein or its analogue of being attached to of the present invention other protein or the factor of fragment or derivative.

(v) as mentioned above, also can be with RAP-2 protein, its analogue, fragment or derivative are used as immunogen (antigen) to produce specific protein.These antibody also can be used for from cell extract or generation RAP-2 protein, its analogue or segmental clone purifying RAP-2 protein (for example RAP-2 or any abnormal shape) from transforming.In addition, these antibody can be used for diagnosing FAS-R part or the TNF system that relates to the RIP mediation of abnormal function with discriminating, or RIP activity independently, for example the specific cell effect mediation by RIP or RIP self makes a living or the low FAS-R part of living or the disorder of TNF-inductive cytosis.Therefore, such disorder should relate to participate in rip protein or various other, the multi-functional intracellular signal formation system of aforesaid RIP-conjugated protein or RAP-2 protein itself, antibody is as the important diagnostic instrument like this.

Should be noted that and utilize any standard screening program of knowing to carry out proteinic separation of RAP-2 of the present invention and discriminating and qualitative, for example, one of these screening procedures, two hybridization programs of yeast, as hereinafter listing, can be used for differentiating rip protein (referring to people such as for example Stanger, 1995) and various RAP-2 protein of the present invention subsequently (except various other the new protein of top and the patent application of examining that has altogether described below).Similar with as mentioned and hereinafter described, various programs can be used for for example affinity chromatography, DNA hybridization program like those skilled in that art known with separate, differentiate with RAP-2 protein of the present invention qualitatively or with separate, discriminating and qualitative other protein, the factor, acceptors etc., it can be attached to RAP-2 protein of the present invention.

As mentioned above, RAP-2 protein can be used to produce specificity, for example RAP-2 and its abnormal shape in the proteinic antibody of RAP-2.Therefore can use these antibody or fragment, as hereinafter listing in detail, should be understood that in these applications its antibody or fragment be specificity in RAP-2 proteinic those.

Therefore be attached to RIP specifically and be mediation agent/conditioning agent of RIP based on analysis of the present invention: RAP-2, therefore independent or mediate/be adjusted in inflammation with RIP with mode that other protein concurs, the activity of RIP in necrocytosis or the cell survival approach (FAS-R in the necrocytosis approach for example, p55-R, MORT-1, MACH, Mch4, TRAF2 in G1 and TRADD or the cell survival approach), the interaction that RAP-2-RIP can be strengthened or develop to design is important, as needs, and depend on that these approach are to interact by RAP-2-RIP to strengthen, suppress.Such medicine is helpful to numerous disease.For other, there is the acute hepatitis of acute loss as if to reflect the hepatocellular death that FAS-R is ligand-mediated to liver; The necrocytosis of autoimmunity inductive is the death of the β Langerhans cell of pancreas for example, causes diabetes; The death of the cell of transplant rejection (for example, kidney, heart and liver); Death at the oligodendroglia of multiple sclerosis deutocerebrum.

RAP-2 or one or more its possible abnormal shape are possible and therefore they are used as the specific inhibitor of RIP recited above at the inhibitor that one or more above-mentioned approach is used as RIP " natural ".Equally, also can screen for example peptide of other material, organic compound, antibody or the like is to obtain the suppressing interactional specific drugs of RAP-2-RIP.

Non--restriction embodiment is based on forefathers to the substrate specificity of the inhibitor peptides of ICE or the similar proteolytic enzyme of ICE and ICE with utilize peptide synthetic epitope analysis, and this embodiment is to design and screen to the interactional inhibitor peptides of RAP-2-RIP.Discovery by ICE effectively four amino acid of the most basic requirement design of cleavage of peptide have cracking site (people such as Sleath, 1990 of enough methylamines in the P1 position to stay in the P1 position and to have to amino acid whose powerful hobby; People such as Howard, 1991; People such as Thornberry, 1992).In addition, the fluorogenic reactant peptide (a kind of tetrapeptide), acetyl-Asp-Glu-Val-Asp-a-(4-methyl-coumaryl-7-acid amides) is abbreviated as Ac-DEVD-AMC, be equivalent to the sequence in poly-poly (ADP-ribose) polysaccharase (PARP), discovery is after FAS-R stimulates, and other process of cell death is separated (Kaufmann, 1989 afterwards soon at cell; People such as Kaufmann, 1993; People such as Lazebnik, 1994) with by CPP32 (many CED3/ICE proteolytic enzyme families) and the cracking effectively of MACH proteolytic enzyme (with also GI proteolytic enzyme for example similarly, the IL 120367 in examining that for example owns together).

Because at the locational Asp of the P1 of substrate being important, the Asp and the tetrapeptide in three initial residue positions that have as the residue of tetramino acid can be screened apace to be attached to the position of protease activities, for example utilize Geysen (Geysen, 1985; People such as Geysen, 1987) method of development is wherein screened to find the special interaction with antibody the peptide on many solid support things.By multiple detection method well known by persons skilled in the art, can survey in conjunction with MACH1 proteolytic enzyme to special peptide as G1 proteolytic enzyme etc.The method that shows this Geysen ' s can be at least 4000 peptides of every workday test.

Can illustrate accurate calmodulin binding domain CaM of interaction or homology zone between decision RAP-2 and the RIP in a similar fashion, peptide can be screened to interact as retardance then, for example have similar in appearance to the synthetic peptide of the order in calmodulin binding domain CaM or its complementary zone, described complementary region and natural RAP-2 competition combine with RIP's.

Can will can suppress that molecule that the inflammation of RAP-2 or the active medicine of necrocytosis or inhibitor peptides and promotion enter cell combines by the interaction that suppresses RAP-2-RIP or compound.

United States Patent (USP) 5,149,782 disclose molecule to be transported passes molecule of cytolemma coupling to film mixture such as membrane polypeptides, and ionic channel forms polypeptide, other membrane polypeptides, the acid of long-chain fat, for example palmitinic acid.These film mixtures enter tenuigenin with the film lipid bilayer and the promotion of the conjugates insertion cell of molecule.

People such as Low, United States Patent (USP) 5,108, such as but not limited to protein, active principle is striden the effective means that film discharges in the born of the same parents of nucleic acid by receptors mediation for molecule in 921 comments.These receptor systems comprise the identification semi-lactosi, seminose, and mannose-6-phosphate, Transferrins,iron complexes, transcobalamin (vitamin B12), the big sphaeroprotein of α-2, Regular Insulin and other peptide growth factor be the somatomedin of epidermis (EGF) for example.People such as Low instruction is owing to stride film transportation with multiplicity with related receptors mediation at the vitamin H on the surface of most cell and the position of folate receptor, the acceptor of nutrition, biological example acceptor plain and folate can be advantageously used in strengthens passing the cytolemma transportation.Therefore contact the film of striding that begins receptors mediation and transport mechanism waiting to discharge into the complex compound that forms between cytoplasmic compound and part biological example element or the folate and carry vitamin H or folate receptor, thereby the compound that allows to want enters cell.

In addition, the known peptide order that will want of those skilled in that art makes " chimeric peptide " to be transported pass cytolemma with leading/signal peptide sequence fusion with preparation " chimeric peptide " and enters tenuigenin.

The technician will recognize that in the peptide field, and the interactional inhibitor peptides of RAP-2-RIP of the present invention comprises the simulating peptide medicine or also can rapid screening be attached to RAP-2/RIP proteolytic enzyme with the more stable inhibitor of design.

Can recognize that also the aforesaid transportation that is used to help or strengthen inhibitor peptides to pass cytolemma is used for RAP-2 or its special-shaped itself and other plays peptide and the protein that acts in the born of the same parents.

With regard to antibody mentioned in this article, term " antibody " is meant and comprises polyclonal antibody, monoclonal antibody (mAbs), chimeric antibody, anti-idiotypic is (anti--Id) antibody, described antibody can be solubility or carry out mark in the bonded mode, and by any technology but be not limited to enzymatic lysis, the fragment that peptide is synthetic or recombinant technology provides.

Polyclonal antibody is the heterogeneous population that derives from the antibody molecule of the animal serum of immunogen immunization.Monoclonal antibody contains the basically allogenic colony of specificity in antigenic antibody, and similar epi-position binding site is contained basically in described colony.Adopt the known method antigen of those skilled in that art to obtain mAbs.Referring to, for example Kohler and Milstain, natural 256:495-497 (1975); United States Patent (USP) 4,376,110; People such as Ausubel, Harlow and Lane antibody: laboratory manual, cold spring harbor laboratory (1988); With people such as Colligan, present immunology scheme, Greene publishes association and Wiley Interscience N.Y. (1992-1996), and its all the elements are incorporated herein by reference.Such antibody can comprise IgG, IgM, IgE, IgA, the immunoglobulin (Ig) kind of GILD and its subspecies.Can be with the hybridoma that produces mAb of the present invention external, original position or culturing in vivo.In the body or the high generation of tiring of original position be effective production method at present.

Chimeric antibody is the molecule that different piece derives from different animal species, for example has the variable region and the human normal immunoglobulin invariant region that derive from mouse mAb.At first chimeric antibody is used for reducing immunogenicity and increasing output in application, for example, when the mAbs of mouse has high yield from hybridoma, but when higher immunogenicity is arranged in the people, chimeric mAbs that like this can end user/mouse.Chimeric antibody that is used to produce and method are known (people such as Cabilly, Proc.Natl.Acad.Sci.USA 81:3273.3277 (1984) of those skilled in that art; People such as Morrison, Proc.Natl.Acad.Sci.USA 81:6851-6855 (1984); People such as Boulianne, natural 312:643-646 (1984); People such as Cabilly, european patent application 125023 (open day 1984.11.14); People such as Neuberger, natural 314:268-270 (1985); People such as Taniguchi, european patent application 171496 (open day 1985.02.19); People such as Morrison, european patent application 173494 (open day 1986.03.05); People such as Neuberger, International Patent Application WO 8601533, (open day 1986.03.13); People such as Kudo, european patent application 184187 (open day 1986.06.11); People such as Sahagan, Journal of Immunology 137:1066-1074 (1986); People such as Robinson, International Patent Application WO 8702671 (open day 1987.05.07); People such as Liu, Proc.Natl.Acad.Sci USA84:3439-3443 (1987); People such as Sun, Proc.Natl.Acad.Sci USA84:214-218 (1987); People such as Better, science 240:1041-1043 (1988); With Harlow and Lane, antibody: laboratory manual sees above.These are with reference to being incorporated herein as reference fully.

Anti--idiotypic (anti--Id) antibody is the identification antibody of the decision family of the uniqueness related with the antigen binding site of antibody usually.The animal (for example mouse strain) of the type by identical kind of immunization and heredity prepares Id antibody as the source of the mAb of the anti-Id that is preparing.Will discern and respond the decision family of the antibody of immunization by antibody (anti--Id antibody) animal of immunoprophylaxis that produces these idiotypic decision families.Referring to United States Patent (USP) 4,699, No. 880, the document is incorporated herein by reference fully.

Also will resist-Id antibody is used as " immunogen " with the replying of another animal induction of immunity, produce so-called anti--anti--Id antibody.Should anti--anti--its epi-position of Id be entirely identical to the primary mAb that induces anti-Id.Therefore, the antibody of the idiotypic epi-position by utilizing anti-mAb, the clone of other of the specific antibody that recognition expression is same is possible.

Therefore, produce anti-RAP-2 protein of the present invention, analogue, fragment, the mAbs of derivative is used on the suitable animal, for example induces anti--Id-antibody in the BALB/c mouse.The spleen cell that will come from the mouse of immunity is used to produce anti-hybridoma excretory and resists-Id mAbs.To resist in addition ,-Id mAbs is coupled to for example keyhole hemocyanin (KLH) and be used for the other BALB/c mouse of immunization of carrier.The serum that obtains from these mouse contains anti--anti--Id antibody, and this antibody has top RAP-2 protein, analogue, fragment, the primary mAb that the epi-position of derivative is special in conjunction with attribute.

Therefore anti--Id mAbs have himself the idiotypic epi-position or similar in " idiotopes " epi-position to be illustrated, for example GRB protein-a.

Term " antibody " also be meant comprise complete molecule with and fragment, for example Fab and F (ab ') ₂, it can conjugated antigen.Fab and F (ab ') ₂Fragment lacks the Fc fragment of complete antibody, clearly can participate in circulation more quickly and have the non-specific tissue lower than complete antibody people such as [, nucleic acid method magazine 24:316-325 (1983)] Wahl.

Will understand the method Fab and the F (ab ') that are used for complete antibody molecule according to disclosed herein ₂Be used for that other fragment of antibody of the present invention can be used for detecting and quantitative RAP-2 protein.Use enzyme for example papoid (to produce the Fab fragment) or stomach en-[to produce F (ab ') ₂Fragment], by the such fragment of the typical production of proteolysed division.

It is said that antibody is the molecule of a kind of " competent combination ", if thereby competent specifically reacting with this molecule combines this molecule to antibody.Term " epi-position " is meant competent and any molecular moiety antibodies, this part also can be by that antibody recognition, usually epi-position or antigen decision family is by the chemically active surface grouping of molecule, for example amino acid or sugared side chain and the characteristic of special three-dimensional structure and special charge characteristic are arranged.

" antigen " is meant the molecule or the part molecule of competent binding antibody, and in addition, its competent induced animal is produced the competent antibody that is attached to that antigenic epi-position.Antigen can have one or more epi-positions.Above-mentioned special reaction is that indication antigen will be with the mode of high selectivity and corresponding antibody and do not react with the majority of other antibody, and this antibody is caused by other antigen.

To be used for antibody of the present invention, antibody fragment is used for quantitatively or qualitatively surveying RAP-2 protein or surveying the existence of expressing the proteinic cell of RAP-2 of the present invention at sample.Be coupled to the antibody mediated immunity fluorescence technique of the fluorized marking of light microscope by use, the wandering cells counter, or luminescent counter detects and finishes.

Antibody of the present invention (or fragment) from histological immunofluorescence technique or the immune microscope of being used as, is detected RAP-2 protein of the present invention with original position.Finish that original position detects and the antibody of mark of the present invention is offered such sample by the sample of learning from patient's moving tissue.By using or covering biological sample so that antibody to be provided better by antibody (or fragment) with sign.By using such program, not only measure the proteinic existence of RAP-2, and it can be distributed in the tissue of being checked.The present invention can make, and those skilled in the art will readily understand that the histological method (for example dyeing procedure) of general kind can be modified so that detection arrives at the destination in position.

Typically be used for the biological sample of the following cultivation of antibody existence that the proteinic test pack of RAP-2 of the present invention is contained in the proteinic sign of competent identification RAP-2, the liquid that biological example is learned, tissue extract, recently for example lymphocyte or white cell or the cultured cells in tissue culture of Shou Huo cell adopts many technology for detection antibody known in the art.

With solid phase upholder or carrier nitrocellulose for example, or competent fixed cell, cell particle or soluble proteinic other solid support thing are handled biological sample.After with the antibody treatment of detectable label of the present invention, wash upholder or carrier then, as mentioned above with suitable reducing.The second phase is with buffer reagent washing solid phase upholder or carrier, to remove antibody freely then.Adopt conventional means to survey the amount of the bonded sign of solid support thing or carrier then.

" solid phase upholder ", " solid phase support ", " solid support thing ", " solid carrier ", " upholder " or " carrier " refers to the upholder or the antibody of competent conjugated antigen or antibody.Upholder or the carrier known comprise glass, polystyrene, polypropylene, polyethylene, dextran, nylon amylase, natural and the Mierocrystalline cellulose of modifying, polyacrylamide, gabbro, and magnetite.The performance of carrier can be soluble or undissolvable for the objective of the invention is in the degree of a little.Buttress material can in fact can have any possible node configuration, as long as the molecule of coupling has the ability to be attached on antigen or the antibody.Therefore, upholder or carrier configuration can be spheric, and be columniform as pearl, as on the surface, inside of pipe, or the outer surface of rod.Either-or, the surface can be smooth for example flaky test strip or the like.First-selected upholder or carrier comprise polystyrene bead.Those skilled in that art know other suitable carriers with binding antibody or antigen, or utilize normal experiment can determine equally.

The combination that can measure aforesaid many antibody of authorizing of the present invention according to known method is active.Those skilled in that art can clear and definite each test and best implementation condition by routine test.

Other stirs as washing, vibration, and steps such as filtration can be added in the analysis, because be usual or necessary for specific situation.

One of method that can detect ground mark antibody of the present invention is by being connected to enzyme and being used for enzyme immunoassay (ELA).Ought be exposed to suitable substrate material later in turn, this enzyme will react to produce the part of chemistry by this way with reactant, this part is for example by spectrophotometric, the part of fluorometric or the chemistry surveyed by the method for vision.Can be used for to detect the enzyme that indicates antibody and include, but are not limited to malate dehydrogenase, nuclease, δ-5-steroide isomeras, yeast alcohol dehydrogenase, alpha glycerophosphate dehydrogenase, triose phosphate salt isomerase, horseradish peroxidase, the Phosphoric acid esterase of alkalescence, asparaginase, glucose oxidase, beta galactosidase enzyme, rnase, urase, catalase, G-6-P salt dehydrogenase, glucoamylase and acetylcholin-esterase.Finish detection by the colorimetric method, this method is used the reactant of the product look of enzyme.Also can realize detecting by degree with the reaction of the comparison reactant enzyme of the standard vision of similar preparation.

Use multiple other immunoassay realize to detect.For example, adopting the antibody or the antibody fragment of radioactive mark, is possible by using radioimmunoassay (RIA) to survey R-PTPase.At Work, T.S. wait the people, North Holland PublishingCompany, the biology of NY (1978) molecule, found the useful description of RIA in laboratory process method and the biological chemistry, special in by Chard, T., chapter be named as " radioimmunoassay is identified and relevant technology ", be incorporated herein as reference.Adopt the means of similar usage counter or phenomenon scintillometer numeral or radioautography to survey radioactive isotropic substance.

Compound traget antibody with fluorescent of the present invention is possible.When the antibody of fluorized marking contacts with the light of suitable wavelength, survey the fluorescence that occurs then.Normally used fluorescently-labeled compound is a fluorescein isothiocyanate at most, rhodalline, phycoerythrine, pycocyanin, allophycocyanin, o-phthaldehyde and fluorescamine.

The metal of use radiofluorescence is 152E for example, and other lanthanide series also can detect ground mark.Use such metal chelating group these metals to be appended to antibody as the rare triamine pentaacetic of diethyl acid (ETPA).

Also can detect ground mark by antagonist by being coupled to chemiluminescence compound.By detecting chemiluminescent existence, measure the existence of the antibody of chemiluminescent labeling.This chemoluminescence is to occur in the reaction process of chemistry.The example of the compound of spendable especially chemiluminescent labeling is luminol, isoluminol, theromaticacridinium ester, imidazoles, acridinium salt and oxalate.

Similarly, the bioluminescence compound can be used for mark antibody of the present invention.Noclilucence is the chemoluminescence type that is based upon in the biological system, and wherein catalytic protein increases the efficient of chemiluminescence reaction.Measure the existence of bioluminescent protein matter by detecting luminous existence.Important bioluminescent compound is a fluorescein, luciferin enzyme, luciferin enzyme and aequorin.

Antibody molecule of the present invention can adapt to and be used for the immunometric evaluation, and also known " two positions " or " sandwich " analyzed.Analyze at typical immunometric, quantitative unlabelled antibody (or fragment of antibody) is attached on solid support thing or the carrier, the soluble antibody of quantitative detectable mark adds to allow the solid phase antibody, antigen, and the complex compound of the three-state that forms between the antibody of mark detects and/or quantitation.

Typical and first-selected immunometric measures and comprises that " forward " measure, and the antibody that wherein at first will be attached to the solid phase contacts with treating the sample through assaying, and the solid phase antibody-antigen complex compound by the formation two condition is with from sample extraction antigen.After suitable hatching, washing solid support thing or carrier are to remove the residue of liquid sample, comprise unreacted antigen, if desired, contact with the solution of the antibody (function is " acceptor molecule ") of the mark that contains unknown quantity then, after second incubation period, compound by the antibody of unlabelled antibody permission mark with the antigen that is attached to solid support thing or carrier, solid support thing or carrier are washed for the second time to remove the antibody of unreacted mark.

Use " sandwich " type of one again, can use with antigen of the present invention, so-called " simultaneous " and " reverse " measured.Simultaneous mensuration comprises single incubation step, and the antibody that for example will be attached to solid support thing or carrier and mark joins the sample for the treatment of through assaying simultaneously.Hatch finish after, with the washing of solid support thing or carrier with the residue of removing liquid sample and the antibody of compound mark not.Measure the existence of the antibody related of mark then, because it is in routine " forward " sandwich assay with solid support thing or carrier.

In " reverse " measured, after the suitable period of hatching, utilize at first progressively solution to join liquid sample with the antibody of mark, add the unlabelled antibody that is attached to solid support thing or carrier subsequently.After second hatches, wash the antibody freedom of the residue and the unreacted mark of solid mutual-assistance sample in the mode of routine.Go into " simultaneously " and " forward " test then, measure the antibody of the mark related with solid support thing or carrier.

That the recombinant DNA program of employing standard is produced is of the present invention (referring to for example, people such as Sambrook, 1989 and people such as Ansabel, 1987-1995, see above), wherein transform known suitable eucaryon of those skilled in that art or prokaryotic cell prokaryocyte, therefore, the invention still further relates to such expression vector and be used to produce proteinic conversion host of the present invention by suitable eucaryon that contains coded protein or prokaryotic vector.As mentioned above, these protein also comprise the analogue of biologic activity, fragment and derivative, therefore comprise vectors encoding them, also comprise coding these proteinic analogue and fragments, comprising analogue and the segmental host that production is such with the conversion host, is the derivatives that adopt protein or analogue or segmental modification master copy modification production by these proteinic derivatives that transform host's generation.

The invention still further relates to the pharmaceutical composition that comprises the proteinic recombinant animal virus vector of coding RAP-2, this carrier competent special target cell (for example, cancer cells) surface protein that is attached to of also encoding enters the virus surface proteins matter of cell to instruct the RAP-2 protein sequence.Pharmaceutical composition of the present invention in addition comprises (a) antisense sequences oligonucleotide sequence as the coding RAP-2 protein sequence of active composition, or (b) blocks the interactional medicine of RAP-2-RIP.

Pharmaceutical composition of the present invention comprises that the active ingredient of q.s is to obtain the purpose of its plan.In addition, the primer sets compound can contain suitable pharmacology acceptable carrier, this carrier comprises vehicle and auxiliary agent, this helps active compound to be processed into the preparation that can use on pharmacology, and can make such preparation stabilization can be used for patient's administration, as the known technology of those skilled in that art to needs.

Special-shaped or abnormal shape of the shady RAP-2 of being protein and its is expressing the similar mode of various other protein expressions that the described intracellular signal of the patent application of examining that participates in owning together forms approach, expresses in different tissues and obviously has different special-shaped modes with different level significantly.These differences can help tissue specificity feature that Fas/APO1-part and TNF are replied.As other situation (people such as Wang, 1994 of CED3/ICE homology; People such as Alnemri, 1995), inventor's verified in the past (at above-mentioned international patent application) MACH abnormal shape of finding to contain incomplete CED3/1CE zone (for example MACH α 3) to coexpression have MACH α 1 or MACH α 2 molecules are inhibited; Find that also they stop dead inducing by Fas/APO1 and p55-R.Expression in such abnormal shape in the cell has constituted the Cytotoxic cell self-protection of anti-Fas/APOI-and TNF-mediation; the similar inhibition of the also shady abnormal shape of G1 at least is (G1 is recently isolating new Mch4-and possible MACH-conjugated protein, and this protein has MORT conditioning agent and proteolytic enzyme zone-referring to the IL that is examining 120367 that owns together) like this.The specific meticulous coordination of the function that similarly should allow active MACH abnormal shape of the various ununiformity of MACH abnormal shape and same G1 abnormal shape open to suspicion, and analogue also allows active G1 abnormal shape, and wherein ununiformity substantially exceeds the viewed result of other CED3/ICE family.Therefore, as mentioned above, thereby just and the activation of the interaction of RIP and pair cell death or the equilibrated effect between the cell survival approach, RAP-2 protein or possible abnormal shape have different effects in different tissues as mentioned above.

Some RAP-2 abnormal shapes also may have other function.For example, RAP-2 or some RAP-2 abnormal shapes also may have the effect in the site of molecule, and described molecule participates in the non-cell toxicity effect of Fas/APOI and TNF acceptor by means of the effect with the interaction of RIP or independent RIP.

Because Fas/APO1 and TNF acceptor cause inflammation, the ability of the uniqueness of necrocytosis, and the TNF acceptor excites other tissue to damage active ability, departing from of these function of receptors should be harmful especially to organism.Really, verified these acceptors excessive and effectively function help pathological performance (Vassalli, 1992 of various diseases; Nagata and Golstein, 1995).Differentiate that the signal that participates in acceptor forms active molecule and finds that the mode of the discovery of these compounds of adjusting can instruct new treatment approach, others of the present invention are conspicuous from the following examples.

Following non-limiting example and accompanying drawing will be described the present invention in more detail.

Be further noted that following step:

I) two screening by hybridization and two hybridization beta-galactosidase enzymess are expressed test; The (ii) expression of induced protein, metabolic marker and immunoprecipitation; (iii) external combination; (iv) estimate cytotoxicity; (v) Northern sequential analysis, (referring to people such as Boldin, I995b) 2,3 (also referring to people such as Boldin, 1996) and 4, hereinafter, with regard to MORT-1 and aMORT-1 conjugated protein, (for example MACH), and new isolating protein G 1 (referring to IL 120367) can be used for the separation of (having some to revise) the proteinic correspondence of RAP-2 equally, clone and qualitative and clone's of the present invention abnormal shape.Therefore these programs have constituted and have been used to separate the proteinic separation of RAP-2 of the present invention, and clone qualitatively the whole of same program discloses, as applying for the 114th in the Israel that is examining that owns together, 615,114,986,115,319,116588,117,932, with 120367, and the identical or equivalent way detailed description of corresponding PCT application US96/10521.From outside, with regard to NIK protein and its for example interaction between TRAF2 and RIP and other protein of role in the effect that activates NF-B and therefore necrocytosis and in by this cell survival approach of TRAF2, the IL that is examining 117800 that is owning together by the inventor, people such as IL 119133 and Malinin, 1997 detailed descriptions.

Embodiment 1 is attached to the proteinic separation of RAP-2 and the clone of rip protein

Two screening by hybridization, order-checking and preliminary analysis

This utilizes with RIP as two screening by hybridization methods of bait (referring to for example Fields and Song in B cell library, 1989, WO/96/18641) clone of the about 1.5Kb size of separation, this clone 1.5Kb (referring to the arrow of Fig. 1 and Fig. 2) is used to screen phage cDNA library, produce about 2.0Kb clone, sequence is shown in Fig. 1.

By using and 1.5Kb cloned sequence matching E ST, obtain the EST fragment, it has constituted 3 ' terminal (the studying the hereditary Research Genetics Institute of institute) of I.M.A.G.E.consortium clone #41072.Only disclose this brain that derives from fetus the library the clone be positioned at 3 ' and 5 ' two terminal little sequence fragments.After obtaining the clone, with its order-checking and draw these disclosed sequence fragments and contain wrong.Find the clone that its coding region (Fig. 2) is equal to Fig. 1 that is cloned in of order-checking, but show difference at 5 ' non-coding region.Therefore infer the form of the splicing of cDNA or homologous genes.

This sequential analysis demonstration is similar to RAP, RAP-2 protein does not obviously have " dead zone ", it does not have the MORT conditioning agent, it is not similar to the ICE family in proteolytic enzyme zone, it does not have the kinases zone, does not have the TRAF zone (referring to above-mentioned patent application of examining and various references yet, people such as Malinin especially with regard to all signalling approach that are present in the born of the same parents, 1997).Do not find that suitable motif is present in the sequence of agreement, different is that three leucine zippers (LZ)-similarly obstacle distributes along the protein coding zone.Here be called " similar ", because their two comprise leucine to Xie Ansuan, the replacement of methionine(Met) or Isoleucine.Though it has been generally acknowledged that conservatively, the activity that the unclear whether such variation in the leucine zipper zone allows protein to keep its function promptly is attached to other LZ.In conjunction with studies show that RAP-2 is attached to RIP in essence, RAP-2 not can be incorporated into TRADD, MORT-1, p55-R, p75-R and MACH (so far in the research of carrying out).These results support true RAP-2 obviously to remove " dead zone " and MORT conditioning agent.

Therefore as if, RAP-2 is specific RIP-conjugated protein, this protein is with very specific mode effect/be attached to RIP.Therefore, RAP-2 seemingly has important effect in adjusting/mediation of the RIP of inflammation and necrocytosis/cell survival rate approach.

Briefly, obtain the clone of RAP-2 by the cDNA library that utilizes total length RIP to carry out the people B-cell of two screening by hybridization as bait.The RIP sequence can from before the publication registration number that obtains (referring to people such as STANGER, 1995) and be present in the GenBank database be U25994, it is people RIP sequence (also have mouse RIP sequence, registration number is U25995).Utilize this sequence information, suitable PCR-primer is with the OLIGO4TM software design and can come from total RNA human fibroblasts library (utilizing standard program) by utilization corresponding to the dna fragmentation of RIP encoding part and be used as template cDNA and carry out PCR and obtain.Then the encoding part of RIP is cloned into the carrier (Clontech) of pGBT-9 and as above, is used as bait two screening by hybridization programs.In two screening by hybridization methods, obtain and the interactional coding of RIP RIP conjugated protein.

Clone as above is used to screen phage cDNA library and est database.From Fig. 1 and Fig. 2 as can be seen, when 5 '-non-coding sequence not simultaneously, two clones' encoding sequence is identical.Therefore, we may be concerned about and can select to splice greatly form.This clone's the ORF (open reading frame) that has is the 2.0Kb of 1.5Kb, and the molecular weight of protein itself is 50Kd.The aminoacid sequence of the RAP-2 that infers is shown in Fig. 3.

At " dbest " database, the sequence of people's gene group database level 1 and the above-mentioned RAP-2 of GenBank database analysis shows that the RAP-2 sequence is unique (new) sequence, because there is not known sequences to show and the important homology of RAP-2.After IL 123758 submits, the right of priority that this application requires, people (1998) such as Yamaoka S., the characteristic of the cDNA of the proteinic mouse of report coding 48kD is referred to as NEMO (for the conditioning agent of NF-κ B necessity).(referring to background information).

The protein that other database (in silico) retrieval identification FIP-2-has unknown function, it is at first by people such as Li Y. clone (1998, referring to background information).

As from the general arrangement of RAP-2 and FIP-2 sequence [Fig. 3 (B)] as can be seen, whole similar degree is considerably low (so it does not have astonishing: use to scan based on shared algorithm and does not discern this sequence).Homology between RAP-2 and the FIP-2 increases proteinic C-end, 30 amino acid of last effectively sign C-end.Noteworthy is that except the latter's zone, the LZ-motif of inferring of FIP-2 is (different is that leucine/L-Ala is replaced) that keeps in large quantities in RAP-2.

The short cDNA of about 0.5kb in addition also is identified (ID:1469996) and hereinafter it is appointed as Human shrt.This varient comprises the encoding sequence " section " in the several remote zone of " total length " cDNA that originates from 1.5kb, the different montage of the identical gene that may originate from.

The Northern trace (Clontech) of many tissues and the segmental RAP-2 cDNA of 0.9kb BglII-, hybridization analysis draw the RAP-2 mRNA of complicated patterns.Survey magnitude range at＜1kb up to more or less ubiquitous popular 2.5kb and 6kb varient [Fig. 4 (A)]〉at least 5 different mRNAs of 7kb.

The discriminating of the RAP-2 of embodiment 2 mouse

The mouse EST collection of setting up at TIGR similar studies show that 1.6kb (mouse part ID:761011, Fig. 3) cDNA of part may corresponding mouse RAP-2 because in fact from start to finish coding region with the homologue (referring to Fig. 3) that equals (95%) its people.

Yet the difference between RAP-2 of people and mouse and the NEMO sequence is extended the farther place, and this can give the credit to well-regulated kind of intermediary difference clearly.In fact, comparing with comparing with the sequence of mouse of part with total length people's varient only is maximum significant embodiment (Fig. 3) from the RAP-2 of mouse and NEMO sequence at 7 amino acid whose sections that lack in 249 positions of 20.4 with at the 3 amino acid whose insets (111 the KLE in the position) of the open reading frame of NEMO.Yet this causes the activity of proteins function to disappear.In fact the functional attributes of Bao Dao NEMO shows that situation about finding among the people RAP-2 is opposite, though the hierarchical analysis of NEMO is confirmed that it is positioned signalsome.

RIP is attached to RAP-2 in embodiment 3 mammalian cells

HEK-293T in transfection obtains the interactional physiological related further evidence of RAP-2-RIP with the HeLa cell.Really, as the lysate of the HEK-293 from transfection (the ATCC No.CRL 1573) cell of each swimming lane indication of following Fig. 4 B easily co-precipitation and with anti--these two protein of FLAG mAbs (Kodak) immunoprecipitation.Adopt conventional Westen western blot procedure then, with exist [Fig. 4 (B) and the data not shown] of Histidine-RAP-2 in anti--His6 mAbs (Sigma) analysis immunocomplex.Yet the formation of such mixture does not cause the activity of enzyme: to the degree that we can judge by external mixture kinase assays, the RIP of overexpression does not have phosphorylation RAP-2 (not shown).

Carrying out binding analysis test is attached to any other known intracellular signal and forms protein to measure RAP-2 whether.These the test in to protein TRADD), MORT-1, p55-R, p75-R, MACH are attached to the ability of RAP-2 and test.But, find that RAP-2 not can be incorporated into these protein.RAP-2 is not attached to for example lamin of any control protein, cyclin D yet.

Therefore all above-mentioned results show that new RAP-2 protein may interact in very special mode and special conditioning agent/mediator agent of similarly representing RIP.

Embodiment 4 RAP-2 and NIK interact and control NF-κ B and c-Jun-dependent transcription

Although in two hybridization tests of the HEK-293T mammalian cell of the test of the yeast transfection that shows stable this complex compound of formation, do not find the interaction of RAP-2-NIK.Describe as embodiment 3 and to survey NIK-RAP-2 and interact, just will resist-FLAG antibody is used for Western, then with anti--His6 immunoprecipitation [Fig. 4 (C)].Such difference between yeast and the mammalian cell is not surprising, and when expressing in yeast, total length NIK is easy to let alone in conjunction with attribute.

Consider the fact believes in RIP and the NIK body it is the indispensable conditioning agent of activatory that TNF-induces NF-KB.Whether we check that the overexpression of RAP-2 can not be interfered specific signalling approach in cell culture.The experimental group that begins in the HEK-293T cell with the of short duration transfection of reporter's plasmid, described plasmid comprise the luciferase gene under the basic promotor control of HIV-LTR.In similar setting, set up the RAP-2 downward modulation at first, almost retreat into basic level, signalling (the NIK that relates to TNF by various known NF-κ B inductors, TRAF2, the processing of reportorial activation that overexpression RIP etc.) causes and outside stimulus [TNF and PMA, Fig. 5 (A)] pair cell.(for NF-κ B (5A) is HIVLTR-LUC or CMV-LUC with the report plasmid, for c-Jun (5B) activation experiment is GAL4-LUC), with the interim transfection HEK-293T cell of plasmid (pcRAP-2) for the expression plasmid and the empty plasmid (pcDNA3) of described inductor or the total length RAP-2 that encodes.Clearly, the fact is: RAP-2 can bring into play its effect, and up to the dropping signal transduction pathway, the effect that can hint this proteinic part is to various, and dispersive, and signal formation approach is common (referring to above).Simultaneously, it is not [Fig. 5 (A)] of contradiction that the κ B-of luciferase independently transcribes (CMA early stage start promotor), so we believe and can control by basic the transcribing of RAP-2/the translate possible rearrangement of mechanism.These results are proved (not shown) subsequently in the HeLa cell.

But, titrimetry shows as further tiring, actual phenomenon is more complicated, in fact, pcRAP-2 with various amounts is shown in Fig. 6, TRAF2 is the expression in the HEK-293T cell temporarily, and RAP-2 sharply changes its behavior when lower concentration (about 20 nanograms/106 cells), strengthens TRAF2 NF-κ B inductive and transcribes [referring to Fig. 6 (A)].But, by replacing the primary inset with opposite direction, the carrier of called after RAP-2 antisense expression, pcRAP-2-a/s (antisense) construct TRAF2 with various different amounts is expressed in the HEK-293T cell provisionally, analyze the effect of disappearance gradually of RAP-2, cause making concentration dependent figure.The amount of the RAP-2 DNA that replys rough and transfection of total trend indicator cells of slope is inversely proportional to, and different is that " the zero "-point (Fig. 6) corresponding to this proteinic endogenous level is dropped in the characteristic zone.Should be noted that by importing the given expression of gene of antisense downward modulation be more accurate, as opposite with the overexpression that justice is arranged.In fact, antisense does not participate in external proteinic artificial production in the cell, and therefore, clearly the validity of the ability that RAP-2 is suppressed is rule down below.Yet, should be noted that the above-mentioned sudden turn of events reflects with low concentration, non-reversing ground, half of the anti-meaning of chart (Fig. 6).

In order to evaluate the diversity of re-reading system, wherein relate to RAP-2, we change into research c-Jun, and a kind of factor of nuclear proves that it is setting up and safeguarding that suitable urgent effect of replying is almost with NF-κ B no less important.Utilize the composition of commercial " approach detection " system (Stratgene), at HEK-293T and HeLa cell [referring to Fig. 5 (B) and Fig. 6 (B)] we confirm activator with the AP-1 of several approvals relevant similar two aspect behavior.

Embodiment 5 RAP-2 strengthen the super phosphorylation of c-Jun, do not change the JNK activity

In order to study the mechanism that has deep effect to transcribing, it is necessary measuring the normal broken accurate level of signaling.The trans activation possibility of c-Jun of generally acknowledging be by two serine residues of the activating area of the end of its amino ( ⁶³Ser﹠amp; ⁷³Ser) extracellular signal inductive phosphorylation is regulated.The JNK/SAPK protein kinase of responsible phosphorylation above-mentioned constitutes the subclass far away of map kinase family and itself exists via the further upstream dual kinase mediated kinases of specificity specificity ¹⁸³Thr and ¹⁸⁵The Tyr phosphorylation activates.Therefore, the phosphorylation of the suitable position in c-Jun and the JNKs can be used as the mark of the proteinic state of activation of reflection.The Western engram analysis shows that with the lysate of the HEK-293T cell of of short duration transfection though the weakening of transcribing of c-Jun-mediation, RAP-2 strengthens endogenous c-Jun significantly and exists ⁶³Ser is by many thing inductive phosphorylations [seeing Fig. 7 (A)] that irritate.Constituting thing with the expression of indication is represented by Fig. 7 in the lysate with total cell of the HEK-293T cell of pcDNA3-carrier transfection, by negative sign (-) or in identical figure plus sige represent pcRAP-2, on SDS-PAGE, separate, transfer to the ECL-film and with anti--phospho- ⁶³Ser-c-Jun Abs (NEB) surveys.Be shown on the low list of Fig. 7 A this film with anti-total-c-Jun Abs resets in contrast and looks into (NEB).

Yet the raising that the total amount of c-Jun keeps the level of c-Jun to keep steady is originated as possible modification.Be specific to the antibody of the phosphorylation form of JNK1/2, not detecting with the kinase whose amount of the activatory of RAP-2 overexpression has substantial increase, shows that the additional phosphorylation of c-Jun does not result from the JNKs activity [Fig. 7 (B)] of the dependent raising of RAP-2-.By the total phospho-of having of Western trace ( ¹⁸³Thr/ ¹⁸⁵Tyr)-lysate of JNKAbs (NEB) shows as Fig. 7, surveys the period that the activatory JNK1/2 cell from the HEK-293T cell of pCDNA3 that handles with hrTNF α activation JNK1/2 or pcRAP-2 transfection increases progressively.

In the further support of back one idea, carry out the vitro kinase test with the GST-c-Jun of sedimentary JNK1 of immunity and purification as reactant and produce identical result [Fig. 7 (C)] in essence.With empty carrier, pcRAP-2 and pcRIP produce the ability that purify GST-Jun with HA-JNK1-expression plasmid cotransfection HEK-293T cell via playing the terminal HA-tag immunoprecipitation of N-and measuring its bacterium phosphorylation by 32P-incorporation in an in vitro kinase assay with various.By SDS-PAGE analytical reaction product, as be shown in Fig. 7.

When the HEK293 of transfection cellular immunization precipitation RAP-2-IKK1 complex compound, this complex compound is cultivated under external phosphorylation situation, RAP-2 becomes phosphorylation.The effect of the function of the phosphorylation of RAP-2 studies show that activation in the sudden change cancellation Jun phosphorylation of the specific Serine of this protein (in the position 148) family.Illustrate as Figure 13, when the overexpression of wild type RAP-2 causes a large amount of increase of Jun phosphorylation to the RAP-2 overexpression, (S148A) this does not influence the phosphorylation of Jun fully.RAP2 is not subjected to the influence of this sudden change fully to the influence of NF-KB.These investigation results show that the phosphorylation of the Serine 148 of RAP-2 specifically relates to its effect to the JUN phosphorylation.

Embodiment 6 RAP-2 do not suppress c-Jun and ReIA is attached to DNA

Consider true: the experiment of embodiment 5 reports does not show the target that the cytosolic of the RAP-2 overexpression of NF-κ B and AP-1 signalling cascade regulates, and it is essential that the integrity that we investigate the process of nuclear is transcribed.The Electro mobility change of carrying out with the extracting solution of the nuclear of the HEK-293T cell of transfection is analyzed (EMSA) clear and definite proof RAP-2 and is not disturbed c-Jun and RelA to be attached to oligonucleotide (Fig. 8) corresponding to the recognition sequence of standard.In fact, aware the effectiveness that the DNA/AP-1 mixture forms in the RAP-2 cells transfected and increase several times.In addition, between RAP-2 and c-Jun/RelA, do not observe interaction and cause the latter's activating area sterical obstacle.The enhanser that acts on that this hint RAP-2 enters nuclear is hit by target in conjunction with some position in the downstream that occurs.

Interact in the body of embodiment 7 RAP-2 and histone acetyltransferase TIP60

TIP60 (GeneBank U 74667) belongs to the family of the nucleoprotein of nearest description, is called as histone acetyltransferase (HATs).The activity of these proteinic enzymes is relevant with the state of the chromatin Structure of nucleosomal complexes.The speed that HATs transcribes with the some element associated of rerecording device and the modulation of having the ability frequently.By when vicinity begins, loosening chromatin HATs effect by means of the lysine residue of ethanoyl being transferred to histone.Thereby promote the various relevant factors to enter DNA.Obviously one of these complementary nucleus protein want to promote the intersection between enhanser binding factor and the dna polymerase i I to talk.Therefore we investigate, and TIP60 and RAP-2 are compound.From the immunoprecipitation of HeLa cell, carry out two hybridization test result demonstration RAP-2 and TIP60 subsequently and in two systems, interact intensely.Yet according to the coexpression in the HEK-293T cell, we do not have to see the suitable change to the influence of NF-κ B and c-Jun of RAP-2 mediation.What stimulate promptly in control test that TIP60 (w/o RAP-2) observes similarly loses variation, produce conclusion: the short time reads (after the transfection 20-30 hour) and perhaps gets rid of report DNA and enter the chance that becomes dyeing materialization, and remaining time enough is so that the similar enzyme of HAT-works.

Embodiment 8 clone #10-and the new protein of RAP-2 mutual restriction

As the total length RAP-2 protein of bait, we have separated and the clone #10 hereinafter that is expressed as RAP-2 or clone's #10-encoded protein matter or RAT-bonded protein #10 or RBP-10 (Figure 10) in two screening by hybridization in the cDNA library of B-cell.The new protein of mutual restriction.Find that the MW on primary clone (about 2.2kb) coded surface is the polypeptide of the supposition of 60kDa.Yet the initial codon of the ATG that infers is lost from this sequence apparently.Although its sizable length, therefore the cDNA that obtains is further to 5 ' terminal expansion to reconstitute whole open reading frame.

Two hybrids mensuration demonstrations this protein except that RAP-2 in conjunction with repertoire of clone #10 has the suitable intensive avidity with TRAP2.Clone #10 is not attached to RIP, TRADD, MORT1, MACH, TNFR-I, TIP60 and NIK and be attached to several control proteins (for example lamin and cyclin).But can get rid of clone #10 and may reside in mammalian cell with combining of NIK, the odd habit of the behavior of considering in yeast.Proof clone #10 is attached to RAP-2 in 200 each amino acid of the latter's C-end, promptly with RIP, and TIP60, NIK and IKK β are in conjunction with dispensable zone.

Clone #10 and the TRAF-2 coexpression in the 293T cell in Mammals stops the activation of the NF-κ B of TRAF2-mediation, and the coexpression of clone #10 and NIK has been improved NF-κ B forcefully by the latter activation.The important regulatory function of these investigation result indications clone #10.Observed different regulating effect perhaps hints and has different non-overlapped protein where-useds in the cell.

Several targets of GenBank are caused producing identification F40F12.5 (number of registering on the books S42834)-from the protein of the hypotetical of C.Elegans, wherein assigning does not have physiological effect in the touring seeking of the approaching RBP-10-homologue of identification.Interesting, find that F40F12.5 demonstration and several members of the proteolytic enzyme family of protecting the ubiquitin-guidance that is subjected to widely have similarity.These enzyme equilibriums the destructive effect of ubiquitination machine, known its accuse more than half protein degradation in cell.And the ubiquitin ligase enzyme is responsible for poly--ubiquitin tree is attached to the protein of predetermined degraded, and ubiquitin proteolytic enzyme stops the tree of growing up effectively to send out branch.Yet such supposition of the function of the homophylic F40F12.5 of the proteolytic enzyme that instructs based on proteolytic enzyme and top ubiquitin is seemingly suspicious, similarly also do not detect particular proteins whether and have enzymic activity the ubiquitin polymkeric substance, in addition, as if such coincidence fully unlikely takes place a pair of viewpoint:

A) residue that it is believed that formation core catalysis region in the subclass of ubiquitin proteolytic enzyme is not guarded at F40F12.5 with in RBP-10;

B) ubiquitin except the various kind that originates from instructs the catalytic site (from the bacterium to people) of the enzyme of proteolytic enzyme family in fact not have the display sequence similarity, and F40F12.5 and clone #10 show the homology of reliable degree.

The protein of the mutual restriction of embodiment 9 clone #84:RAP-2

By in two screening by hybridization in the cDNA library that is applied in the B-cell as the total length RAP-2 protein of bait, we have separated the bonded protein of other RAP-2, and be called clone #84.

Find that clone #84 specifically is attached to total length RAP-2, and with the protein TRAF2 of other analysis, MORT1, TRADD, RIP, NIK, TIP60 and Lamin do not have display interaction.Find the part 5 of clone #84 '-sequence is entirely identical to the previous clone's of the in check protein C GR19 of encode cell growth cDNA sequence, be identified as in the p53 that carries function proteinic (people 1996 such as Madden S., #U66469 registers on the books) cell specifically transcript to adjusted.The CGR19 of sequential analysis causes at it-and stub area discerned C3HC4-Zink and referred to motif (being also referred to as RING refers to).Find the growth of the several clones of expression inhibiting of CGR19.May regulate in check network of cell cycle by the member of TNF-R family by being attached to RAP-2 proteinic involving of CGR19 in the adjusting of NF-κ B.

Structure-function relationship of embodiment 10 RAP-2

A. calmodulin binding domain CaM

By using the successive deletion analysis, to the mapping of the calmodulin binding domain CaM in the RAP-2 with discerned RIP, NIK, TIP60-in conjunction with and self-associated region (Figure 11).

To the RAP-2 that is attached to RIP proteinic zone mapping, finish between amino acid/11 77-218 and at amino acid 264 in this zone.

So far do not find IKK β and NIK binding site (amino acid 95-264) and (amino acid/11-264) overlapping RIP ' s binding site RAP-2 (Figure 11) in RAP-2 respectively.

Be attached to TIP60 apparently in zone mapping across amino acid 95-264.With interact most across the deletion fragment of amino acid 95-309 might be the result of the special encumbrance conformation of the disappearance that belongs to specific.

Can notice that it is attached to the similar difference of the clone #10 RAP-2 related with being attached to the oneself being attached to deletion fragment.Yet opposite with TIP60, the fact is the deletion fragment that total length RAP-2 is attached to the deletion fragment that contains amino acid 218-416 and comprises amino acid/11-264, and hint relates to the zone location of the highest dimerization between amino acid 217-264.

By clone's #10 encoded protein matter, have above-mentioned exception, be combined in apparently and start from amino acid 218-309 zone and terminate in amino acid 416, therefore, its binding site can comprise and has RIP, NIK, the overlapping region of the binding site of IKK β and TIP60 (Figure 11).

B. the zone of function

The degree of our present knowledge, all functions in same zone to RAP-2 are mapped (being called the super phosphorylation that NF-κ B suppresses and induces c-Jun) (Figure 11).

The zone location of the effective adjusting of signalling that in addition, may be by all inductors that is used to test is in the N-of this protein fragments end.

Therefore the zone that is comprised by amino acid 95-416 produces effect, though compare obviously more weakly with being caused by complete protein, is produced by the gathering of endogenous RAP-2.

And except RelA, the effect of all inductors that are used to test is by the amino acid mediation of little 100 N-ends to about RAP-2.In fact, comprise the different effect of fragment mediation of amino acid/11-102, although Shi Du [Figure 12 (B)] considerably.

On the other hand, the RAP-2 protein of the longer part of derived need of the success of RelA.So far we stipulate the line of delimitation between this zone amino acid/11-264, give on the surface have the specific RelA-association of a part in conjunction with the zone between the amino acid/11 57-264 of attribute.

C. combination-function relationship

According to the result who is shown in Figure 11 and Figure 12, it seems:

A) except RelA, for this proteinic function, be attached to the RAP-2 of RIP, clone #10 and maximum possible is attached to NIK and TIP60 is unessential is as the inhibition of overexpression inductive NF-κ B.

B) RAP-2 is mediated by different binding events significantly at least in part to the activatory effect of inducing of ReIA overexpression.In essence, find that all above-mentioned protein can help the activity of arranging, for example from the test inference of carrying out so far.

Interactional accurate position between RAP-2 and the RIP has to be determined so far, as if but this position is to be specific to RIP and RAP-2, known with other not in the interactive protein of RIP MORT-1 for example, TRADD, FAS-R and also TRAF2 (see people such as Malinin, 1997) share, also occur (according to sequential analysis with above-mentioned different database sequence relatively) RAP-2 do not have ' dead zone ', MORTMODULE, a proteolytic enzyme zone (for example ICE/CED3 motif), kinases zone/motif/do not have TRAF zone.At this circuit, biological activation analysis shows that also RAP-2 obviously has following characteristic:

(i) served as scale and reached, RAP-2 is by TNF or by TRADD, RIP, and TRAF-2, NIK or p65 NF-κ B subunit suppress the activation of NF-κ B forcefully,

(ii) RAP-2 strengthens the super phosphorylation of c-Jun, does not change the activity of JNK.

(iii) the RAP-2 that shows as deletion analysis does not need the dead zone of RIP, does not need the kinase activity of RIP so that be attached to RIP yet;

(iv) based on above-mentioned deletion analysis, the zone that RAP-2 is attached to RIP is reduced to 200 amino acid whose N-stub areas;

(RAP-2 is attached to NIK v) in mammalian cell, rather than in yeast.

Consider the seemingly very special RIP conjugated protein of above-mentioned RAP-2 and so possible interior signalling approach of born of the same parents that relates to the RIP-mediation of RIP conditioning agent/mediator agent.

Based on above-mentioned conclusion, show that RAP-2 participates in the active adjusting of RIP/mediation.Ground in the born of the same parents, these RIP participate in cell survival approach (NF-kB activation, may via with the interaction of TRAF2) and participate in inflammation and necrocytosis approach (independently via its ' dead zone ' or via with other protein MORT-1 for example, TRADD, p55-R, the interaction and for example MACH of FAS-R and related proteolytic enzyme, Mch4, G1 etc.).Wherein RAP-2 can modulate/mediate the active possible method of RIP in above detailed description.For example the interaction of RAP-2-RIP can be directed at the enhancing of necrocytosis or cell survival approach, or can cell guiding death or the inhibition of cell survival approach, this reinforcement or suppress to depend on member's the activity of relevant other of approach in these two opposite born of the same parents.RAP-2 also can have the proteinic work of docking in order to RIP molecule and other the RIP-or the gathering of RAP-2 conjugated protein to be provided, based on other member's live vol of these approach in the cell, its aggregate has function in the direction of necrocytosis or cell survival (or even both) then.

The Polyclonal Antibody Preparation of embodiment 11 anti-RAP-2

At first with the pure preparation subcutaneous injection rabbit of 5 microgram RAP-2, said preparation is emulsifiable in by RAP-2 that Freund auxiliary agent completely obtains.After three weeks, inject rabbit again so that the pure preparation of 5 microgram RAP-2 is subcutaneous, said preparation was emulsifiable in by RAP-2 that incomplete Freund auxiliary agent obtains, with two other RAP-2 that are dissolved in PBS of intervals injection of 10 days.After last immunity, got blood from rabbit in 10 days.Then show antibody horizontal with the radioimmunoassay Faxian.With the RAP-2 of 125I-sign and the various dilution of rabbit serum (1: 50,1: 500,1: 5,000 and 1: 50,000) mixing.In total volume 200 microlitres, add protein-G agarose pearl (20 microlitres, suspension Pharmacia).At room temperature this mixture was placed 1 hour, washed pearl then 3 times, count bound radioactivity.The rabbit antiserum(antisera) of anti-people leptin is used as negative contrast, compares with the contrast of feminine gender and measure tiring of RAP-2.

The MONOCLONAL ANTIBODIES SPECIFIC FOR of embodiment 12 anti-RAP-2

At first the emulsion with the auxiliary agent of Freund completely of 2 micrograms purifies RAP-2 injection jenny Balb/C mouse (3 months big) really, after three weeks, with the subcutaneous injection of incomplete Freund auxiliary agent, with 10 days intervals to be dissolved in three other subcutaneous injections of PBS.The endoperitoneal last increase injection in 4 days and 3 days before being fused to mouse, the highest combination of measuring as IRIA of demonstration tire (vide infra).Use is from merging as the spleen of the animal of fusion partners and the ready myeloma clone of lymphoglandula and lymphocyte.The cell distribution that merges is arrived little culture plate, with in the DMEM that has replenished HAT and 15% horse serum, select hybridoma, with the hybridoma that is found the antibody that produces anti-RAP-2 through the dilution process subclone of restriction be expelled to the Balb/C mouse, this mouse with the pristane perfusion so that produce ascites.The isotype of the ELISA test kit regulation antibody that use is commercial (Amersham, UK).

The following screening of carrying out the hybridoma of the monoclonal antibody that produces anti-RAP-2: through being inverted the anti-RAP-2 antibody that exists in solid phase radioimmunoassay (IRIA) the test hybridoma supernatant liquid.With the IL-18BPa-His6 of Talon-purifying (10 micrograms/ml, the bag of 100 microlitres/well) by elisa plate (Dynatech Laboratories, Alexandria, VA).After 4 degree are hatched whole night, wash dull and stereotyped twice with the PBS that contains BSA (0.5%) and Tween20 (0.05%), be closed in washing soln minimum 2 hours, 37 degree add hybridoma culture supernatant liquid (100 microlitres/well) and should cultivating 4 hours at 37 ℃ by flat board.Wash this flat board 3 times and at room temperature add goat-anti--mouse horseradish peroxidase (HRP, Jackson Labs, 1: 10, the conjugates of 000,100 microlitre/well) 2 hours.With flat board washing 4 times and by ABTS (2,2 '-azino-bis (3-ethyibenzthiazoline-6-sulfonicac acid, Sigma) and H ₂O ₂Develop the color as substrate.Read this flat board by automatic ELISA reader.The sample of the acquisition OD higher at least 5 times than negative control value is considered to male.

Employing affinity layer is clear to be used for purifying RAP-2 with RAP-2 antibody.

Embodiment 13 ELISA test

Wrap by droplet plate (Dynatech or Maxisorb byNunc) with anti--RAP-2 monoclonal antibody (the hybridoma supernatant liquor or the ascites liquid immunoglobulin (Ig) that do not have serum) at 4 ℃.Dull and stereotyped with the PBS washing that contains BSA (0.5%) and Tween20 (0.05%), be closed in identical solution minimum 2 hours, 37 degree join wells (100 microlitres/well) 4 hours, 37 ℃, should wash 3 times with the PBS that contains Tween20 (0.05%) by flat board.Resist in 4 degree interpolations-RAP-2 serum (1: 1000,100 microlitres/, should wash 3 times by flat board well) with further overnight incubation, at room temperature add goat-anti--mouse horseradish peroxidase (HRP, Jackson Labs, 1: 10, the conjugates of 000,100 microlitre/well) 2 hours.With flat board washing 4 times and by ABTS (2.2 '-azino-bis (3-ethylbenzthiazoline-6-sulfonic acid, Sigma) and H ₂O ₂Develop the color as substrate.Read this flat board by automatic ELISA reader.

All described the present invention now, those skilled in that art understand the parameter of the Equivalent of wide scope, and concentration and situation can be carried out equally, do not deviate from the spirit and scope of invention and do not have the over-drastic experiment.

When describing in conjunction with specific embodiments when of the present invention, can do further modification to the present invention.Usually according to principle plan of the present invention this application is covered any variation of the present invention, use, or adapt to and comprise and depart from content disclosed by the invention, as known in the art or the custom practice, wherein relate to the present invention and as can be applied to, according to the characteristic of scope necessity proposed above of hereinafter accessory claim.

Ji Zai all references herein, comprise magazine article or summary, the patent application of the disclosed or corresponding U.S. or the foreign country authorized by the U.S. or other reference all are incorporated herein by reference, and are included in all data in the reference of record, form, figure and text.In addition, the full content at the reference that is recorded in this paper is incorporated herein by reference.

With reference to known method steps, conventional method steps, known method or conventional method disapprove with any method open, instruct or advise any aspect of the present invention, specification sheets or embodiment.

Previously described specific embodiment shows the comprehensive person's character of the present invention fully, comprise that by the knowledge of using those skilled in that art the content of appended reference is easy to modify and/or adapt to the specific embodiment of various application, do not need the over-drastic experiment, do not deviate from universal of the present invention.Therefore, plan is included in the coordinator of meaning and the scope of disclosed embodiment with such adaptation and modification, based on instruction described herein and guidance.The wording or the term that will be understood that this paper are for purpose of description, are not in order to limit invention, so the term of this specification sheets or wording is by instruction and the guidance of skilled skilled worker according to this paper, make an explanation in conjunction with those of ordinary skills' knowledge.

Reference

Alnemri, people such as E.S. (1995) journal of biological chemistry 270:4312-4317.

Barinaga, M. (1993) science 262:1512-1514.

Beg, A.A. and Baltimore, D. science 274:782-784.

Beidler, people such as J., (1995) biological chemistry 270:16526-16528.

Berger, people such as J. (1988) gene 66:1-10.

Beutler, B. and Cerami, C. (1987) NEJM:316:379-385.

Bigda, people such as J. (1994) experimental methodology magazine 180:445-460.

Boldin, people such as M.P. (1995a) journal of biological chemistry 270:337-341.

Boldin, people such as M.P. (1995b) journal of biological chemistry 270:7795-7798.

Boldin, people such as M.P. (1996) cell 85:803-815.

Brakebusch, people such as C. (1992) EMBOJ., 11:943-950.

Brockhaus, people such as M. (1990) the annual report 87:3127-3131 of American Academy of Sciences.

Cantor, people such as G.H. (1993) the annual report 90:10932-6 of American Academy of Sciences.

Cerreti, people such as D.P. (1992) science 256:97-100.

Chen, people such as C.J. (1992) the annual report 660:271-3 of American Academy of Sciences.

People such as Chinnaiyan (1995) cell 81:505-512.

People such as Chinnaiyan (1996) journal of biological chemistry 271:4961-4965.

Cifone, people such as M.G. (1995) EMBOJ.14:5859-5868.

Clement, people such as M.V. (1994) The Journal of Experimental Medicine 180:557-567.

Crisell, people such as P. (1993) nucleic acids research (Britain) 21 (22): 5251-5.

Present molecular biology scheme (Ausubel, F.M., Brent, R., Kingston, R.E., Moore, D.D., Seidman, J.G., Smith, J.A., Struhl, K., Albright, L.M., Coen, D.M.﹠amp; Varki, A., eds.), (1994) pp.8.1.1-8.1.6 and 16.7-16.7.8, Greene combined publication company of society and Wiley ﹠amp; Sons company, New York.

Dirks, W. waits the people, (1993) gene 128:247-249.

Durfee, people such as T. (1993) gene development 7:555-569.

Eischen, people such as C.M. (1994) Journal of Immunology 153:1947-1954.

Ellis, people such as H.M. (1986) cell 44:817-829.

Enari, the natural 375:78-81 of people such as M. (1995).

Engelmann, people such as H. (1990) journal of biological chemistry 265:1531-1536.

Faucheu, people such as C. (1995) EMBOJ.14:1914～1922.

Fernandes-Alnemri, people such as T. (1994) journal of biological chemistry 269:30761-30764.

Fernandes-Alnemri, people such as T. (1995) cancer research 55:2737-2742.

Fernandes-Alnemri, people such as T. (1996) the annual report 93:7464-7469 of American Academy of Sciences.

Field, people such as J. (1988) molecular cytobiology 8:2159-2165.

Fields, S. and Song, the natural 340:245-246 of O. (1989).

Frangioni, J.V. and Neel, B.G. (1993) biochemical analysis 210:179-187.

Geysen, the immunology 6:364-369 of H.M. (1985) today.

Geysen, people such as H.M. (1987) immunization method magazine 102:259-274.

Gossen, M. and Boujard, H. (1992) American Academy of Sciences annual report, 89:5547-5551.

Grell, the European Journal of Immunology 24:2563-2566 of people such as M. (1994).

Heller, people such as R.A. (1990) the annual report 87:6151-6155 of American Academy of Sciences.

Henkart, P.A. (1996) immunity 4:195-201.

Hohmann, people such as H.-P. (1989) journal of biological chemistry 264:14927-14934.

Howard, people such as A.D. (1991) Journal of Immunology 147:2964-2969.

Hsu, people such as H. (1995) cell 81:495-504.

Hsu, people such as H. (1996) cell 84:299-308.

Itoh, people such as N. (1991) cell 66:233.

Itoh, N. and Nagata, S. (1993) journal of biological chemistry 268:10932-7.

Joseph, S. and Burke, J.M. (1993) journal of biological chemistry 268:24515-8.

Kamens, people such as J. (1995) journal of biological chemistry 270:15250-15256.

Kaufmann, S.H. (1989) cancer research 49:5870-5878.

Kaufmann, S.H. (1993) cancer research 53:3976-3985.

Kischkel, people such as F.C. (1995) EMBOJ.14:5579-5588.

Koizumi, biomedical (Japan) 16 (9): the 879-83 of people such as M. (1993).

Kumar, people such as S. (1994) gene development 8:1613-1626.

Kumar, S. (1995) biological chemistry science trend 20:198-202.

Lazebnik, the natural 371:346-347 of people such as Y.A. (1994).

Leithauser, people such as F. (1993) laboratory Investment Principles 69:415-429.

Li, people such as Y. (1998) molecular cytobiology 18:1601-1610.

Loetscher, people such as H. (1990) cell 61:351-359.

Los, the natural 375:81-83 of people such as M. (1995).

Madden, people such as S.L. (1996) cancer research 56:5384-5390.

Malinin, the natural 385:540-544 of people such as N.L. (1997).

Martin, people such as S.J. (1995) journal of biological chemistry 270:6425-6428.

Mashima, people such as T. (1995) biological chemistry biophysics research communication 209:907-915.

Miller, people such as B.E. (1995) Journal of Immunology 154:1331-1338.

Milligan, people such as C.E. (1995) neuroscience 15:385-393.

Miura, people such as M. (1995) the annual report 92:8318-8322 of American Academy of Sciences.

Munday, people such as N.A. (1995) journal of biological chemistry 270:15870-15876.

Muranishi, people such as S. (1991) drug research 8:649.

MustiAM waits people (1997) science 1997 275:400-402.

Nagata, S. and Golstein, P. (1995) science 267,1449-1456.

Natoli, people such as G. (1997) journal of biological chemistry 272,26079-26082.

Nicholson, the natural 376:37-43 of people such as D.W. (1995).

Nophar, people such as Y. (1990) EMBOJ., 9:3269-3278.

Piquet, people such as P.F. (1987) The Journal of Experimental Medicine 166:1280-89.

People such as Ray (1992) cell 69:597-604.

Ruggiero, people such as V. (1987) cellular immunology 107:317-325.

People such as Sambrook (1989) molecular cloning: laboratory manual, press of cold spring harbor laboratory, cold spring port, New York.

Schall, people such as T.J. (1990) cell, 61:361-370.

People such as Schlegel (1996) journal of biological chemistry 271:1841-1844.

Schulze-Osthoff, people such as K. (1994) EMBOJ.13:4587-4596.

Shimayama, people such as T. (1993) Nucleic Acids Symp.Ser.29:177-8.

Shore, people such as S.K. (1993) oncogene 8:3183-8.

Sleath, people such as P.R. (1990) biological chemistry 265:14526-14528.

Smith, people such as C.A. (1990) science 248:1019-1023.

Song, people such as H.Y. (1994) journal of biological chemistry 269:22492-22495.

Srinivasula, people such as S.M. (1996) Proc.NatI.Acad.Sci. U.S. 93:14486-14491.

Stanger, people such as B.Z. (1995) cell 81:513-523.

Tartaglia, people such as L.A. (1993) cell 74:845-853.

Tewari, people such as M. (1995) journal of biological chemistry 270:3255-3260.

Tewari, people such as M. (1995a) journal of biological chemistry 270:18738-18741.

Tewari, people such as M. (1995b) cell 81:1-20.

Thornberry, the natural 356:768-774 of people such as N.A. (1992).

Thornberry, people such as N.A. (1994) Biochemistry 33:3934-3940.

Tracey, the natural 330:662-664 of people such as J.T. (1987).

Van Antwerp, people such as D.J. (1996) science 274:787-789.

Vandenabeele, people such as P. (1995) cytobiology trend 5:392-400.

Vassalli，P.(1992)Ann.Rev.Immunol.10：411-452。

Wallach, D. (1984) Journal of Immunology 132:2464-9.

Wallach, D. (1986) referring to: Interferon, rabbit 7 (Ion Gresser, ed.), PP.83-122, academic press, London.

Wallach, people such as D. (1994) cytokine 6:556.

Wang, people such as L. (1994) cell 78:739-750.

Wang, people such as C.Y. (1996) science 274:784-787.

Watanabe-Fukunaga, the natural 356:314-317 of people such as R. (1992).

Watanabe, people such as F.R. (1992) Journal of Immunology 148:1274-1279.

Weitzen, people such as M. (1980) Journal of Immunology 125:719-724.

Wilks, people such as A.F. (1989) the annual report 86:1603-1607 of American Academy of Sciences.

People such as Wong (1994) Journal of Immunology 152:1751-1755.

Xue, the natural 377:248-251 of people such as D. (1995).

Yamaoka, people such as S. (1998) cell 95:1231-1240.

Yonehara, people such as S. (1989) experimental technique magazine 169:1747-1756.

Yuan, people such as J. (1993) cell 75:641-652.

Zaccharia, the European pharmacology magazine of people such as S. (1991) 203:353-357.

Zhao, J.J. and Pick, L. (1993) nature (Britain) 365:448-51.

Sequence table

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Yeda researches and develops company limited

＜120〉conditioning agent of the function of TNF/NGF receptor family and other proteinic acceptor

＜130〉TNF/NGF acceptor

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ctggagggtc?gggcccgggc?ggccagcgag?caggcgcggc?agctggagag?tgagcgcgag 720

gcgctgcagc?agcagcacag?cgtgcaggtg?gaccagctgc?gcatgcaggg?ccagagcgtg 780

gaggccgcgc?tccgcatgga?gcgccaggcc?gcctcggagg?agaagaggaa?gctggcccag 840

ttgcaggtgg?cctatcacca?gctcttccaa?gaatacgaca?accacatcaa?gagcagcgtg 900

gtgggcagtg?agcggaagcg?aggaatgcag?ctggaagatc?tcaaacagca?gctccagcag 960

gccgaggagg?ccctggtggc?caaacaggag?gtgatcgata?agctgaagga?ggaggccgag 1020

cagcacaaga?ttgtgatgga?gaccgttccg?gtgctgaagg?cccaggcgga?tatctacaag 1080

gcggacttcc?aggctgagag?gcaggcccgg?gagaagctgg?ccgagaagaa?ggagctcctg 1140

caggagcagc?tggagcagct?gcagagggag?tacagcaaac?tgaaggccag?ctgtcaggag 1200

tcggccagga?tcgaggacat?gaggaagcgg?catgtcgagg?tctcccaggc?ccccttgccc 1260

cccgcccctg?cctacctctc?ctctcccctg?gccctgccca?gccagaggag?gagccccccc 1320

gaggagccac?ctgacttctg?ctgtcccaag?tgccagtatc?aggcccctga?tatggacacc 1380

ctgcagatac?atgtcatgga?gtgcattgag?tagggccggc?cagtgcaagg?ccactgcctg 1440

ccgaggacgt?gcccgggacc?gtgcagtctg?cgctttcctc?tcccgcctgc?ctagcccagg 1500

atgaagggct?gggtggccac?aactgggatg?ccacctggag?ccccacccag?gagctggccg 1560

cggcacctta?cgcttcagct?gttgattccg?ctggtcccct?cttttggggt?agatgcggcc 1620

ccgatcaggc?ctgactcgct?gctctttttg?ttcccttctg?tctgctcgaa?ccacttgcct 1680

cgggctaatc?cctccctctt?cctccacccg?gcactgggga?agtcaagaat?ggggcctggg 1740

gctctcaggg?agaactgctt?cccctggcag?agctgggtgg?cagctcttcc?tcccaccgga 1800

caccgacccg?cccgctgctg?tgccctggga?gtgctgccct?cttaccatgc?acacgggtgc 1860

tctccttttg?ggctgcatgc?tattccattt?tgcagccaga?ccgatgtgta?tttaaccagt 1920

cactattgat?ggacatttgg?gttgtttccc?atctttttgt?taccatmaat?artggcmtag 1980

akaaaatcc?ttgtgcatta?aaaaaaaaa 2009

<210>2

<211>2034

<212>DNA

＜213〉people

<400>2

ttctactcct?ccctcctcct?cactgcgggg?tctgacccta?ctccttgtgt?gaggactcct 60

ctagttcaga?gacatattct?gttcaccaaa?cttgactgcg?ctctatcgag?gtcgttaaat 120

tcttcggaaa?tgcctcacat?atagtttggc?agctagccct?tgccctgttg?gatgaatagg 180

cacctctgga?agagccaact?gtgtgagatg?gtgcagccca?gtggtggccc?ggcagcagat 240

caggacgtac?tgggcgaaga?gtctcctctg?gggaagccag?ccatgctgca?cctgccttca 300

gaacagggcg?ctcctgagac?cctccagcgc?tgcctgggag?gagaatcaag?agctccgaga 360

tgccatccgg?cagtagcaac?cagattcttg?cgggagctgc?cgaagggagc?tttctgcatt 420

ttccaagcca?gccagaggga?ggagaaggag?ttcctcatgt?gcaagttcca?ggaggccagg 480

aaactggtgg?agagactcgg?cctggagaag?ctcgatctga?agaggcagaa?ggagcaggct 540

ctgcgggagg?tggagcacct?gaagagatgc?cagcagcaga?tggctgagga?caaggcctct 600

gtgaaagccc?aggtgacgtc?cttgctcggg?gagctgcagg?agagccagag?tcgcttggag 660

gctgccacta?aggaatgcca?ggctctggag?ggtcgggccc?gggcggccag?cgagcaggcg 720

cggcagctgg?agagtgagcg?cgaggcgctg?cagcagcagc?acagcgtgca?ggtggaccag 780

ctgcgcatgc?agggccagag?cgtggaggcc?gcgctccgca?tggagcgcca?ggccgcctcg 840

gaggagaaga?ggaagctggc?ccagttgcag?gtggcctatc?accagctctt?ccaagaatac 900

gacaaccaca?tcaagagcag?cgtggtgggc?agtgagcgga?agcgaggaat?gcagctggaa 960

gatctcaaac?agcagctcca?gcaggccgag?gaggccctgg?tggccaaaca?ggaggtgatc 1020

gataagctga?aggaggaggc?cgagcagcac?aagattgtga?tggagaccgt?tccggtgctg 1080

aaggcccagg?cggatatcta?caaggcggac?ttccaggctg?agaggcaggc?ccgggagaag 1140

ctggccgaga?agaaggagct?cctgcaggag?cagctggagc?agctgcagag?ggagtacagc 1200

aaactgaagg?ccagctgtca?ggagtcggcc?aggatcgagg?acatgaggaa?gcggcatgtc 1260

gaggtctccc?aggccccctt?gccccccgcc?cctgcctacc?tctcctctcc?cctggccctg 1320

cccagccaga?ggaggagccc?ccccgaggag?ccacctgact?tctgctgtcc?caagtgccag 1380

tatcaggccc?ctgatatgga?caccctgcag?atacatgtca?tggagtgcat?tgagtagggc 1440

cggccagtgc?aaggccactg?cctgccgagg?acgtgcccgg?gaccgtgcag?tctgcgcttt 1500

cctctcccgc?ctgcctagcc?caggatgaag?ggctgggtgg?ccacaactgg?gatgccacct 1560

ggagccccac?ccaggagctg?gccgcggcac?cttacgcttc?agctgttgat?tccgctggtc 1620

ccctcttttg?gggtagatgc?ggccccgatc?aggcctgact?cgctgctctt?tttgttccct 1680

tctgtctgct?cgaaccactt?gcctcgggct?aatccctccc?tcttcctcca?cccggcactg 1740

gggaagtcaa?gaatggggcc?tggggctctc?agggagaact?gcttcccctg?gcagagctgg 1800

gtggcagctc?ttcctcccac?cggacaccga?cccgcccgct?gctgtgccct?gggagtgctg 1860

ccctcttacc?atgcacacgg?gtgctctcct?tttgggctgc?atgctattcc?attttgcagc 1920

cagaccgatg?tgtatttaac?cagtcactat?tgatggacat?ttgggttgtt?tcccatcttt 1980

ttgttaccat?maatartggc?mtagakaaaa?atccttgtgc?attaaaaaaa?aaaa 2034

<210>3

<211>2116

<212>DNA

＜213〉people

<400>3

gccacgaagg?cccagacttt?gaccgttctt?caccaccact?ccagcctcct?cctgtgaact 60

cactgaccac?cgagaacaga?ttccactctt?taccattcag?tctcaccaag?atgcccaata 120

ccaatggaag?tattggccac?agtccacttt?ctctgtcagc?ccagtctgta?atggaagagc 180

taaacactgc?acccgtccaa?gagagtccac?ccttggccat?gcctcctggg?aactcacatg 240

gtctagaagt?gggctcattg?gctgaagtta?aggagaaccc?tcctttctat?ggggtaatcc 300

gttggatcgg?tcagccacca?ggactgaatg?aagtgctcgc?tggactggaa?ctggaagatg 360

agtgtgcagg?ctgtacggat?ggaaccttca?gaggcactcg?gtatttcacc?tgtgccctga 420

agaaggcgct?gtttgtgaaa?ctgaagagct?gcaggcctga?ctctaggttt?gcatcattgc 480

agccggtttc?caatcaagat?tgagcgctgt?aactctttag?catttggagg?ctacttaagt 540

gaagtagtga?agaaaatact?ccaccaaaaa?tggaaaaaga?argcttggag?ataatgattg 600

gggaaagaag?aaaggcatcc?aagggtcatt?acaattcttg?ktacttagac?tcaaccttat 660

tctkgcttat?ttkgctttta?gttctgttct?nggacactgg?tgttacttta?gaccccaaag 720

aaaaagaaac?gatgttagaa?tattwtwkwg?mmacccaaga?gctactgagg?acagaaattg 780

ttaatcctct?gagaatatat?ggatatgtgt?gtgccacaaa?aattatgaaa?ctgaggaaaa 840

tacttgaaaa?ggtggaggct?gcatcaggat?ttacctctga?agaaaaagat?cctgaggaat 900

tcttgaatat?tctgtttcat?catattttaa?gggtagaacc?tttgctaaaa?ataagatcag 960

caggtcaaaa?ggtacaagat?tgttacttct?atcaaatttt?tatggaaaaa?aatgagaaag 1020

ttggcgttcc?cacaattcag?cagttgttag?aatggtcttt?tatcaacagt?aacctgaaat 1080

ttgcagaggc?accatcatgt?ctgattattc?agatgcctcg?atttggaaaa?gactttaaac 1140

tatttaaaaa?atttttcctt?ctctggaatt?agatataaca?gatttacttg?aagacacccc 1200

agacagtgcc?ggatatgtgg?agggcttgca?atgtatgagt?gtaagaatgc?tacgacgatc 1260

cggacaccag?ctggaaaaac?aagcagtttt?gtaaaacctg?caacactcaa?gtccaccttc 1320

atccgaagag?gctgaatcat?aaatataacc?cagtgtcact?ccccaaagac?ttaccccgac 1380

tgggagattg?gagacacggc?tgcatccctt?gccagaatat?ggagttattt?gctgttctct 1440

gcatagaaac?aagccactat?gttgcttttg?tgaagtatgg?gaaggacgat?tctgcctggc 1500

tcttctttgg?acagcatggc?cgatccggga?tggtggtcag?aatggctcaa?cattccccca 1560

agtcmcccmt?gscccagaag?taggagagta?cttggaagat?gtctcctgga?agaccctgaa 1620

wtyccttgga?ctcccaggag?aatcccaagg?ctgtgcacga?agactgcttt?gtgatgccat 1680

atatgtgcca?tgtacccaga?gtccaacaat?gagtttgtac?aaataactgg?gggtcatcgg 1740

gaaaggcaaa?gaaactggaa?ggcagagtcc?ctaacgttgc?atcttattcg?gagctggcag 1800

ttctgttcac?ggtccattgc?cggcaatgga?tgtctttgtg?gtgatgatcc?ttcagaaaag 1860

gatgcctctg?tttaaaaaca?aattgctttt?gtgtccctga?agtatttaat?aagaagcatt 1920

ttgcactcta?gaaagtatgt?ttgtgttggt?tttttaagaa?gtctaaatga?agttattaat 1980

acctgaagct?ttaagttaag?tgcattgatc?atatgatatt?tttggaagca?tacaatttta 2040

attgtggaag?tttaaagcct?cttttagtcc?attgagaatg?taaataaatg?tgtcttcttt 2100

atggaaaaaa?aaaaaa 2116

Claims

1. coding RIP-related protein-2RAP-2 protein DNA sequence, wherein RAP-2 protein can be attached to RIP, and described dna sequence dna comprises one of the following:

(a) sequence as shown in Figure 1;

(b) fragments sequence in the coding (a); Or

(c) sequence of coding (a) or analogue (b), this (a) or analogue (b) are compared to have in aminoacid sequence with (a) or protein (b) and are no more than 10 variation, described each be changed to one and amino acid whosely substitute, remove and/or insert separately, described fragment or analogue can be attached to RIP.

2. coding RAP-2 protein DNA sequence according to claim 1, wherein RAP-2 protein can be attached to RIP, and described dna sequence dna is made of Nucleotide 154-1410 shown in Figure 1 or its fragment.

3. reproducible expression vector comprises claim 1 or 2 described dna sequence dnas.

4. reproducible expression vector according to claim 3, other dna sequence dna that it can be operationally connected to conventional control sequence, promotor or allow to express with correct direction.

5. reproducible expression vector according to claim 3 can be expressed in eukaryotic cell.

6. reproducible expression vector according to claim 3 can be expressed in prokaryotic cell prokaryocyte.

7. eucaryon of Zhuan Huaing or prokaryotic host cell contain each described reproducible expression vector in the claim 3～6.

8. a RAP-2 protein or its fragment by claim 1 or 2 described dna sequence encodings, can be attached to RIP.

9. RAP-2 protein according to claim 8 or its fragment, can regulate or mediate activity in the RIP born of the same parents of RIP in inflammation, cell survival or necrocytosis approach, wherein RIP is by directly or indirectly combining these approach of participation with the interior conditioning agent or the mediation agent of these approach.

10. RAP-2 protein according to claim 8 or its fragment, wherein said protein or its fragment have aminoacid sequence shown in Figure 3.

11. each described RAP-2 protein or its segmental method in the production claim 8～10, be included in and be applicable to the described transformed host cell of conversion claim 7 under the described protein of expression or its segmental condition, modification after realization is translated, obtaining described protein or its fragment, and separate described expressed protein or its fragment.

12. antibody has specificity with each described RAP-2 protein or its fragment in the claim 8～10.

13. according to Claim 8～10 each described RAP-2 protein or its fragment preparation be used for regulating or mediate RIP regulates or the born of the same parents to inflammation, necrocytosis or cell survival approach of mediation in the purposes of the medicine that acts on.

14. each described RAP-2 protein or its fragment are used for the treatment of purposes in the medicine of the cell that tumour cell or HIV infect in preparation according to Claim 8～10.

15. antibody according to claim 12 is used for regulating the purposes of medicine of effect of the pair cell of RIP adjusting/mediation in preparation.

16. regulate the pharmaceutical composition of the effect of RIP pair cell, comprise as each described RAP-2 protein, its biological active fragment or its mixture in the claim 8～10 at least of active ingredient.

17. regulate the pharmaceutical composition of the effect of RIP pair cell, comprise that coding can be in conjunction with the recombinant animal virus vector of each described RAP-2 protein, biological active fragment in the protein of cell surface receptor and the claim 8～10 of encoding.

18. regulate the pharmaceutical composition of the effect of RIP pair cell, comprise oligonucleotide sequence as the antisense sequences of the coding claim 1 of active ingredient or 2 described RAP-2 protein DNA sequences.

19. the proteinic fragment of each described RAP-2 according to Claim 8～10, this fragment is a peptide.